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💵 Salary
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🏢 Precision for Medicine
❌ Clear 14 results
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Project ManagerPrecision for Medicine💰 $60k - $110k* |
ManagerEmbeddedTravelMicrosoftManagementLeadSeniorOperationsMarketingNon Tech |
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Precision for MedicineApply now👀 1,253 views ✅ 68 applied (5%)
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Precision for Medicine is hiring a
Remote Project Manager\n\n\nPrecision for Medicine is the first global precision medicine clinical research services organization, purpose-built to improve the clinical research and development process for new therapeutics. Our novel approach integrates clinical operations excellence, with laboratory expertise, and advanced data sciences to inform every step. We apply our expertise to trials at all stages—from early development through approval—with embedded experience in oncology and rare disease. With over 2000 dedicated professionals and 35 offices worldwide, we stand ready to help accelerate life-changing treatments anywhere around the globe. Won’t you join us today as a Clinical Trial Project Manager?\n\nPosition Summary: \n\nThe Project Manager plans, directs, coordinates, and delivers activities for designated clinical-study projects to ensure that project objectives of quality, scope, cost, and time are accomplished. \n\nEssential functions of the job include but are not limited to: \n\n\n* Serve as primary point-of-contact and primary escalation point to the client \n\n* Coordinate and oversees all functional services including external vendors to the established timeline and budget\n\n* Manage the study budget, ensuring project remains within scope and that any out of scope activities are identified and handled as appropriate\n\n* Develop robust and comprehensive project plans, including timelines, to guide all parameters of trial execution with consistency and quality\n\n* Maintain integrated collaboration with clinical operations in the delivery and participates in clinical activities as appropriate. For projects of very limited scope (i.e. number of sites), PM may assume all clinical activities\n\n* Establish tracking metrics to monitor trial and team progress towards project goals\n\n* Prepare project status updates and report on progress to clients and senior management, offering solutions and opportunities as they arise\n\n* Lead team meetings with the client and sets expectations for the project team\n\n* Communicate effectively with client and Precision management to relay protocol/study issues including any deviations and implements necessary actions in response to those issues\n\n* Travel as necessary according to project needs\n\n* Mentor, train, and supervise staff at a functional level\n\n* Assist with review of clinical study reports\n\n* Support business development and marketing activities as appropriate \n\n* Perform other duties as assigned by management\n\n* May participate in review of protocols and other study documentation \n\n* Provides on-going feedback, development and coaching for functional team members including annual performance reviews\n\n\n\n\nQualifications: \n\nMinimum Required: \n\n\n* Bachelor’s degree or equivalent combination of education/experience in science or health-related field. Advanced degree preferred \n\n* Minimum of 3 years of clinical research experience or proven competencies for this position and a minimum of 1 years of leading a project\n\n* Therapeutic experience in oncology \n\n\n\n\nPreferred: \n\n\n* Advanced degree \n\n\n\n\nOther Required: \n\n\n* Experience with Microsoft Office Products (Outlook, Word, Excel, PowerPoint), Microsoft Project \n\n* Excellent communication and interpersonal skills to effectively interface with others in a team setting \n\n* Excellent organizational skills, attention to detail, and a customer service demeanor \n\n* Ability to travel domestically and internationally including overnight stays \n\n\n\n\nCompetencies: \n\n\n* Working knowledge of project management techniques and tools \n\n* Experience working in a cross-functional project management environment \n\n* Fundamental understanding of cross-functional management \n\n* Fundamental understanding of project planning, risk management and change management with an awareness of appropriate escalation \n\n* High level of integrity and must inspire and demand the highest standards from a professional and ethical perspective \n\n* Ability to lead and inspire excellence within a team \n\n* Ability to create an environment where employees have a sense of ownership that will lead to increases in productivity and efficiency \n\n* Results oriented, accountable, motivated and flexible \n\n* Excellent time management, negotiation, critical thinking, decision making, analytical and interpersonal skills \n\n* Excellent presentation, verbal and written communications skills \n\n* Fundamental understanding of project management software \n\n* Experience in pharmaceutical and/or device research required \n\n\n\n\n \n\n \n\n#Salary and compensation\n
No salary data published by company so we estimated salary based on similar jobs related to Travel, Senior, Marketing and Non Tech jobs that are similar:\n\n
$60,000 — $110,000/year\n
\n\n#Benefits\n 💰 401(k)\n\n🌎 Distributed team\n\n⏰ Async\n\n🤓 Vision insurance\n\n🦷 Dental insurance\n\n🚑 Medical insurance\n\n🏖 Unlimited vacation\n\n🏖 Paid time off\n\n📆 4 day workweek\n\n💰 401k matching\n\n🏔 Company retreats\n\n🏬 Coworking budget\n\n📚 Learning budget\n\n💪 Free gym membership\n\n🧘 Mental wellness budget\n\n🖥 Home office budget\n\n🥧 Pay in crypto\n\n🥸 Pseudonymous\n\n💰 Profit sharing\n\n💰 Equity compensation\n\n⬜️ No whiteboard interview\n\n👀 No monitoring system\n\n🚫 No politics at work\n\n🎅 We hire old (and young)\n\n \n\n#Location\nRemote, Oregon, United States
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👉 Please reference you found the job on Remote OK, this helps us get more companies to post here, thanks! |
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Manager Global Clinical MonitoringPrecision for Medicine💰 $140k - $200k* |
ManagerSystemTeachTrainingTechnicalTravelManagementOperationsHealthcare |
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Precision for MedicineApply now👀 661 views ✅ 13 applied (2%)
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Precision for Medicine is hiring a
Remote Manager Global Clinical Monitoring\n\n\nPosition Summary: \n\n\nThe Manager Global Clinical Monitoring (GCM) offers an additional development path for clinical research professionals. Responsibilities are focused on the management and career development of the organization’s Clinical Research Associate (CRA) workforce as well as supporting the development of departmental initiatives to strengthen the quality and productivity of GCM operations. \n\nThis position requires the ability to independently lead, manage, and motivate a team of CRAs (employee and/or consultant) to a standard consistent with Precision for Medicine’s values and overall focus on quality. Specific focus will be to ensure the right resources are assigned to projects and that those resources have the tools necessary to be successful. In addition, this position will provide the CRAs with career development and support, to minimize turnover and maintain high levels of employee satisfaction \n\n\n\n\nEssential functions of the job include but are not limited to: \n\n\nGenerate action plans and provide developmental/strategic oversight to optimize CRA services, with a focus on high quality delivery of individual/team/departmental goals. \n\nAssist with and contribute to project resourcing to ensure proper level and allocation resource is assigned for each project within their hierarchy (with respect to project phase). Update tracking systems and interface with project teams. \n\nCollaborate with the Clinical Team Leads/Clinical Trial Managers and Clinical Operations Management Team to ensure that resource needs and site requirements are met appropriately. \n\nDevelop, mentor, manage and coach CRA staff to progress their skills so that Precision for Medicine quality standards are maintained. Advocate individual career development, and individual responsibility/accountability. \n\nPerform accompanied site visits to assess CRA skills and developmental needs, as well as assist CRAs with project specific issues. \n\nIdentify quality risks and issues and recommend corrective action plans as needed to leadership team to address deficiencies in performance of employees. \n\nEnsure that all staff have the proper resources, training, materials, and access to systems to deliver on the expectations of their position. \n\nEnsure CRAs provide timely and accurate updates of all required administrative material (SOPs, T&E, etc.) on company systems. \n\nWork with the Clinical Operations Management Team to continually improve and enhance CRA expectations and procedures to promote quality, consistency and efficiency in execution. \n\n\n\n\n\nDevelop and maintain metrics pertinent to CRA resource oversight, and work with Clinical Operations Management Team on the evaluation of these metrics. \n\nParticipate in the interview process for new CRAs by conducting CV review and participating in the interviewing process. \n\nConduct on-boarding training for new CRA staff in conjunction with Human Resources, Clinical Training and other functional areas. \n\nRepresent Precision for Medicine in a professional manner \n\nManage CRA staff in accordance with Precision for Medicine’s values and policies. \n\nSecondary responsibilities include assisting with the planning, assigning, and directing of work as well as gathering performance feedback to contribute to appropriate action plans. \n\nPerform other duties as assigned by Leadership \n\n\n\n\nQualifications: \n\nMinimum Required: \n\n\nGraduate, postgraduate, 4-year college degree, or equivalent experience ideally in a scientific or healthcare discipline \n\n\n\n\nOther Required: \n\n\nAt least 7 years or more in clinical operations, data management or related discipline either in CRO or Pharmaceutical industry with a minimum of 5 years onsite monitoring experience. \n\nMonitoring experience includes use of electronic data capture systems as well as paper and electronic medical records. \n\n3-5 years of direct supervisory experience managing CRAs is expected in candidates for this position including: \n\n\n\n\n\nExperience creating effective development programs for clinical staff. \n\nExperience developing evaluation processes, performing gap analysis, and ensuring all clinical staff are properly trained to perform their duties consistent with Precision for Medicine quality standards \n\nAbility to drive and availability for domestic and international travel including overnight stays, with an expectation of travel approximately 25%. \n\n\n\n\nPreferred: \n\n\nExperience in the Therapeutic area/country of the staff assigned to manage \n\n\n\n\nSkills: \n\nCompetencies: \n\n\nDemonstrates mastery knowledge of ICH-GCP, applicable local regulatory requirements, relevant Precision for Medicine SOPs, technical CRA knowledge of all phases of study (including remote monitoring and clinical data review) as well as regulatory guidance. \n\nHigh capacity for Emotional Intelligence and a passion for people management and development. \n\nAs part of overall line management responsibilities, ability to develop training plans and hold personnel accountable to achieving training goals or addressing training needs \n\nDeep knowledge of how clinical research centers operate along with the ability to teach CRAs to solve site and execution related problems at the site level. \n\nDemonstrates understanding and ability to work with EMRs and EDCs \n\nExhibits high self-motivation and is able to work and plan independently as well as in a team environment. \n\nMotivates other members of the project team to meet timelines and project goals. \n\nHighly organized, ability to set priorities and possesses excellent problem-solving skills. \n\nFocuses on continuous improvement, including the ability to make proactive assessments on how to make processes more efficient and people more effective. \n\nUnderstands clinical trials methodology, including a working knowledge of protocols and indications being studied. \n\nAbility to develop, coach and mentor CRA staff. \n\nDemonstrates a high degree of professionalism, as evidenced by punctuality, ability to deliver on commitments, an understanding of the service culture and positive interactions with customers and teammates, including good interpersonal skills. \n\n\n\n\n\nCommunicates both verbally and in written form in an acceptable manner. \n\nConducts formal presentations to a wide variety of audiences including colleagues, investigative staff, and clients with a high level of proficiency. \n\nPossesses practical knowledge of IT tools and systems in use on project teams. \n\nValues system and work ethic consistent with Precision Values and Company Principles \n\n\n\n\n \n\n#Salary and compensation\n
No salary data published by company so we estimated salary based on similar jobs related to Travel and Travel jobs that are similar:\n\n
$140,000 — $200,000/year\n
\n\n#Benefits\n 💰 401(k)\n\n🌎 Distributed team\n\n⏰ Async\n\n🤓 Vision insurance\n\n🦷 Dental insurance\n\n🚑 Medical insurance\n\n🏖 Unlimited vacation\n\n🏖 Paid time off\n\n📆 4 day workweek\n\n💰 401k matching\n\n🏔 Company retreats\n\n🏬 Coworking budget\n\n📚 Learning budget\n\n💪 Free gym membership\n\n🧘 Mental wellness budget\n\n🖥 Home office budget\n\n🥧 Pay in crypto\n\n🥸 Pseudonymous\n\n💰 Profit sharing\n\n💰 Equity compensation\n\n⬜️ No whiteboard interview\n\n👀 No monitoring system\n\n🚫 No politics at work\n\n🎅 We hire old (and young)\n\n \n\n#Location\nRemote, Oregon, United States
Apply for this job
👉 Please reference you found the job on Remote OK, this helps us get more companies to post here, thanks! |
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Clinical Trial ManagerPrecision for Medicine💰 $118k - $163k* |
ManagerDesignTrainingSupportSoftwareTravelLeadOperationalAnalyticsBiotechHealth |
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Precision for MedicineApply now👀 771 views ✅ 7 applied (1%)
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Precision for Medicine is hiring a
Remote Clinical Trial Manager\nWe have current opportunity for an experienced Clinical Trial Manager in Europe! Join our growing team.\n\nPrecision for Medicine is a precision medicine CRO. Precision’s uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs, industry-leading operational and medical experts, advanced biomarker and data analytics solutions, and an unequivocal real passion for rare diseases and oncology, in addition to working across other therapeutic areas.\n\nYou will be the hub of central intelligence for the studies you will be managing, and will lead CRAs and oversee all clinical aspects of your study across multiple countries, ensuring timeline adherence and scope, whilst ensuring quality delivery. We encourage high-energy, dedicated professionals who enjoy a challenge, thrive in the details and flourish in dynamic environments to explore this opportunity. \n\nWe are addressing the challenges facing the research and development of novel compounds in Oncology and are dedicated to positively impacting the health and lives of patients around the world. If you take a consultative approach to trial management, proving to be a valuable partner in the trial operational delivery process, don't miss exploring working with us.\n\nAbout You:\n\n\n* You love having responsibility and a say in how clinical trials are run\n\n* You plan ahead, but have alternative options and a flexible approach\n\n* You are client focused and \n\n* You are well organised and able to manage timelines and shifting priorities, without sacrificing quality.\n\n* You communicate clearly, often and concisely and know that your role is crucial in keeping the trial running smoothly\n\n* You are a master at identifying any risks that threaten projects and handle them resolutely\n\n* You thrive and work with autonomy and ownership to deliver successful outcomes\n\n\n\n\nThe day-to-day role, and how we will support your continued growth:\n\n\n* Management and operational delivery of the clinical elements within a trial including site selection, start-up, enrollment management, site engagement and support, monitoring planning and execution, data cleaning activities and close-out\n\n* Successful execution of assigned trials and ensuring completion of trial deliverables\n\n* Ensure appropriate communication, regulatory documentation, and ongoing oversight of assigned trial(s) by working in close collaboration with other functional team members\n\n* Mentoring and training of team members\n\n* Identify challenges to study timelines/deliverables and offer creative action plans to the team/sponsor\n\n* Lead CRAs as they establish relationships with their sites for high quality oversight of monitoring, regulatory, IP, site payment and overall site correspondence activities\n\n* Maintain team focus on study priorities through efficient cross-functional partnerships and effective communication to achieve the highest level of client satisfaction\n\n\n\n\nQualifications:\n\nMinimum Required:\n\n\n* Bachelor’s degree or equivalent combination of education/experience in science or health-related field, including experience in the field of oncology\n\n\n\n\nOther Required:\n\n\n* Demonstrable experience leading clinical aspects of your studies across multiple countries in a CRO / Pharma or Biotech company (in a dedicated 'clinical lead' role).\n\n* Working knowledge of GCP/ICH guidelines and the clinical development process\n\n* Availability for domestic and international travel including overnight stays\n\n\n\n\nSkills:\n\n\n* Demonstrated computer skills (MS Office, MS Project, PowerPoint) and software experience (CTMS, eTMF, EDC, IXRS)\n\n* Demonstrated ability to develop positive working relationships with internal and external organizations\n\n* Demonstrates core understanding of medical terminology and clinical trial activities as it relates to the execution of a clinical development plan\n\n\n\n\nCompetencies:\n\n\n* Demonstrates mastery knowledge of ICH-GCP, meaningful Precision SOPs, and regulatory guidance, as well as the ability to implement\n\n\n\n\nPrecision medicine is revolutionizing the attack on cancer—and we are passionate about helping you harness its power. We strike tumors on a molecular level using biomarkers to link specific mutations to specific treatments. We combine deep science with deep data from advanced technological platforms, then layer on specialized expertise in the design and execution of targeted, adaptive clinical trials. Ultimately, we deliver robust insights that inform real-time decisions—and optimize the oncology development pathway.\n\n\nAny data provided as a part of this application will be stored in accordance with our Privacy Policy.\n\nPrecision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law. © 2020 Precision Medicine Group, LLC\n\nIf you are an individual with a disability and require a reasonable accommodation to complete any part of the application process, or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at [email protected].\n\n\n \n\n#Salary and compensation\n
No salary data published by company so we estimated salary based on similar jobs related to Design and Travel jobs that are similar:\n\n
$117,500 — $162,500/year\n
\n\n#Benefits\n 💰 401(k)\n\n🌎 Distributed team\n\n⏰ Async\n\n🤓 Vision insurance\n\n🦷 Dental insurance\n\n🚑 Medical insurance\n\n🏖 Unlimited vacation\n\n🏖 Paid time off\n\n📆 4 day workweek\n\n💰 401k matching\n\n🏔 Company retreats\n\n🏬 Coworking budget\n\n📚 Learning budget\n\n💪 Free gym membership\n\n🧘 Mental wellness budget\n\n🖥 Home office budget\n\n🥧 Pay in crypto\n\n🥸 Pseudonymous\n\n💰 Profit sharing\n\n💰 Equity compensation\n\n⬜️ No whiteboard interview\n\n👀 No monitoring system\n\n🚫 No politics at work\n\n🎅 We hire old (and young)\n\n \n\n#Location\nLondon, England, United Kingdom
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👉 Please reference you found the job on Remote OK, this helps us get more companies to post here, thanks! |
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Clinical Trial ManagerPrecision for Medicine💰 $118k - $163k* |
ManagerDesignTrainingSupportSoftwareTravelLeadOperationalAnalyticsBiotechHealth |
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Precision for MedicineApply now👀 1,033 views ✅ 19 applied (2%)
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Precision for Medicine is hiring a
Remote Clinical Trial Manager\nWe have current opportunity for an experienced Clinical Trial Manager in Europe! Join our growing team.\n\nPrecision for Medicine is a precision medicine CRO. Precision’s uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs, industry-leading operational and medical experts, advanced biomarker and data analytics solutions, and an unequivocal real passion for rare diseases and oncology, in addition to working across other therapeutic areas.\n\nYou will be the hub of central intelligence for the studies you will be managing, and will lead CRAs and oversee all clinical aspects of your study across multiple countries, ensuring timeline adherence and scope, whilst ensuring quality delivery. We encourage high-energy, dedicated professionals who enjoy a challenge, thrive in the details and flourish in dynamic environments to explore this opportunity. \n\nWe are addressing the challenges facing the research and development of novel compounds in Oncology and are dedicated to positively impacting the health and lives of patients around the world. If you take a consultative approach to trial management, proving to be a valuable partner in the trial operational delivery process, don't miss exploring working with us.\n\nAbout You:\n\n\n* You love having responsibility and a say in how clinical trials are run\n\n* You plan ahead, but have alternative options and a flexible approach\n\n* You are client focused and \n\n* You are well organised and able to manage timelines and shifting priorities, without sacrificing quality.\n\n* You communicate clearly, often and concisely and know that your role is crucial in keeping the trial running smoothly\n\n* You are a master at identifying any risks that threaten projects and handle them resolutely\n\n* You thrive and work with autonomy and ownership to deliver successful outcomes\n\n\n\n\nThe day-to-day role, and how we will support your continued growth:\n\n\n* Management and operational delivery of the clinical elements within a trial including site selection, start-up, enrollment management, site engagement and support, monitoring planning and execution, data cleaning activities and close-out\n\n* Successful execution of assigned trials and ensuring completion of trial deliverables\n\n* Ensure appropriate communication, regulatory documentation, and ongoing oversight of assigned trial(s) by working in close collaboration with other functional team members\n\n* Mentoring and training of team members\n\n* Identify challenges to study timelines/deliverables and offer creative action plans to the team/sponsor\n\n* Lead CRAs as they establish relationships with their sites for high quality oversight of monitoring, regulatory, IP, site payment and overall site correspondence activities\n\n* Maintain team focus on study priorities through efficient cross-functional partnerships and effective communication to achieve the highest level of client satisfaction\n\n\n\n\nQualifications:\n\nMinimum Required:\n\n\n* Bachelor’s degree or equivalent combination of education/experience in science or health-related field, including experience in the field of oncology\n\n\n\n\nOther Required:\n\n\n* Demonstrable experience leading clinical aspects of your studies across multiple countries in a CRO / Pharma or Biotech company (in a dedicated 'clinical lead' role).\n\n* Working knowledge of GCP/ICH guidelines and the clinical development process\n\n* Availability for domestic and international travel including overnight stays\n\n\n\n\nSkills:\n\n\n* Demonstrated computer skills (MS Office, MS Project, PowerPoint) and software experience (CTMS, eTMF, EDC, IXRS)\n\n* Demonstrated ability to develop positive working relationships with internal and external organizations\n\n* Demonstrates core understanding of medical terminology and clinical trial activities as it relates to the execution of a clinical development plan\n\n\n\n\nCompetencies:\n\n\n* Demonstrates mastery knowledge of ICH-GCP, meaningful Precision SOPs, and regulatory guidance, as well as the ability to implement\n\n\n\n\nPrecision medicine is revolutionizing the attack on cancer—and we are passionate about helping you harness its power. We strike tumors on a molecular level using biomarkers to link specific mutations to specific treatments. We combine deep science with deep data from advanced technological platforms, then layer on specialized expertise in the design and execution of targeted, adaptive clinical trials. Ultimately, we deliver robust insights that inform real-time decisions—and optimize the oncology development pathway.\n\n\nAny data provided as a part of this application will be stored in accordance with our Privacy Policy.\n\nPrecision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law. © 2020 Precision Medicine Group, LLC\n\nIf you are an individual with a disability and require a reasonable accommodation to complete any part of the application process, or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at [email protected].\n\n\n \n\n#Salary and compensation\n
No salary data published by company so we estimated salary based on similar jobs related to Design and Travel jobs that are similar:\n\n
$117,500 — $162,500/year\n
\n\n#Benefits\n 💰 401(k)\n\n🌎 Distributed team\n\n⏰ Async\n\n🤓 Vision insurance\n\n🦷 Dental insurance\n\n🚑 Medical insurance\n\n🏖 Unlimited vacation\n\n🏖 Paid time off\n\n📆 4 day workweek\n\n💰 401k matching\n\n🏔 Company retreats\n\n🏬 Coworking budget\n\n📚 Learning budget\n\n💪 Free gym membership\n\n🧘 Mental wellness budget\n\n🖥 Home office budget\n\n🥧 Pay in crypto\n\n🥸 Pseudonymous\n\n💰 Profit sharing\n\n💰 Equity compensation\n\n⬜️ No whiteboard interview\n\n👀 No monitoring system\n\n🚫 No politics at work\n\n🎅 We hire old (and young)\n\n \n\n#Location\nMadrid, Madrid, Spain
Apply for this job
👉 Please reference you found the job on Remote OK, this helps us get more companies to post here, thanks! |
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Clinical Trial ManagerPrecision for Medicine💰 $118k - $163k* |
ManagerDesignTrainingSupportSoftwareTravelLeadOperationalAnalyticsBiotechHealth |
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Precision for MedicineApply now👀 481 views ✅ 2 applied (0%)
Share this job:
Precision for Medicine is hiring a
Remote Clinical Trial Manager\nWe have current opportunity for an experienced Clinical Trial Manager in Europe! Join our growing team.\n\nPrecision for Medicine is a precision medicine CRO. Precision’s uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs, industry-leading operational and medical experts, advanced biomarker and data analytics solutions, and an unequivocal real passion for rare diseases and oncology, in addition to working across other therapeutic areas.\n\nYou will be the hub of central intelligence for the studies you will be managing, and will lead CRAs and oversee all clinical aspects of your study across multiple countries, ensuring timeline adherence and scope, whilst ensuring quality delivery. We encourage high-energy, dedicated professionals who enjoy a challenge, thrive in the details and flourish in dynamic environments to explore this opportunity. \n\nWe are addressing the challenges facing the research and development of novel compounds in Oncology and are dedicated to positively impacting the health and lives of patients around the world. If you take a consultative approach to trial management, proving to be a valuable partner in the trial operational delivery process, don't miss exploring working with us.\n\nAbout You:\n\n\n* You love having responsibility and a say in how clinical trials are run\n\n* You plan ahead, but have alternative options and a flexible approach\n\n* You are client focused and \n\n* You are well organised and able to manage timelines and shifting priorities, without sacrificing quality.\n\n* You communicate clearly, often and concisely and know that your role is crucial in keeping the trial running smoothly\n\n* You are a master at identifying any risks that threaten projects and handle them resolutely\n\n* You thrive and work with autonomy and ownership to deliver successful outcomes\n\n\n\n\nThe day-to-day role, and how we will support your continued growth:\n\n\n* Management and operational delivery of the clinical elements within a trial including site selection, start-up, enrollment management, site engagement and support, monitoring planning and execution, data cleaning activities and close-out\n\n* Successful execution of assigned trials and ensuring completion of trial deliverables\n\n* Ensure appropriate communication, regulatory documentation, and ongoing oversight of assigned trial(s) by working in close collaboration with other functional team members\n\n* Mentoring and training of team members\n\n* Identify challenges to study timelines/deliverables and offer creative action plans to the team/sponsor\n\n* Lead CRAs as they establish relationships with their sites for high quality oversight of monitoring, regulatory, IP, site payment and overall site correspondence activities\n\n* Maintain team focus on study priorities through efficient cross-functional partnerships and effective communication to achieve the highest level of client satisfaction\n\n\n\n\nQualifications:\n\nMinimum Required:\n\n\n* Bachelor’s degree or equivalent combination of education/experience in science or health-related field, including experience in the field of oncology\n\n\n\n\nOther Required:\n\n\n* Demonstrable experience leading clinical aspects of your studies across multiple countries in a CRO / Pharma or Biotech company (in a dedicated 'clinical lead' role).\n\n* Working knowledge of GCP/ICH guidelines and the clinical development process\n\n* Availability for domestic and international travel including overnight stays\n\n\n\n\nSkills:\n\n\n* Demonstrated computer skills (MS Office, MS Project, PowerPoint) and software experience (CTMS, eTMF, EDC, IXRS)\n\n* Demonstrated ability to develop positive working relationships with internal and external organizations\n\n* Demonstrates core understanding of medical terminology and clinical trial activities as it relates to the execution of a clinical development plan\n\n\n\n\nCompetencies:\n\n\n* Demonstrates mastery knowledge of ICH-GCP, meaningful Precision SOPs, and regulatory guidance, as well as the ability to implement\n\n\n\n\nPrecision medicine is revolutionizing the attack on cancer—and we are passionate about helping you harness its power. We strike tumors on a molecular level using biomarkers to link specific mutations to specific treatments. We combine deep science with deep data from advanced technological platforms, then layer on specialized expertise in the design and execution of targeted, adaptive clinical trials. Ultimately, we deliver robust insights that inform real-time decisions—and optimize the oncology development pathway.\n\n\nAny data provided as a part of this application will be stored in accordance with our Privacy Policy.\n\nPrecision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law. © 2020 Precision Medicine Group, LLC\n\nIf you are an individual with a disability and require a reasonable accommodation to complete any part of the application process, or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at [email protected].\n\n\n \n\n#Salary and compensation\n
No salary data published by company so we estimated salary based on similar jobs related to Design and Travel jobs that are similar:\n\n
$117,500 — $162,500/year\n
\n\n#Benefits\n 💰 401(k)\n\n🌎 Distributed team\n\n⏰ Async\n\n🤓 Vision insurance\n\n🦷 Dental insurance\n\n🚑 Medical insurance\n\n🏖 Unlimited vacation\n\n🏖 Paid time off\n\n📆 4 day workweek\n\n💰 401k matching\n\n🏔 Company retreats\n\n🏬 Coworking budget\n\n📚 Learning budget\n\n💪 Free gym membership\n\n🧘 Mental wellness budget\n\n🖥 Home office budget\n\n🥧 Pay in crypto\n\n🥸 Pseudonymous\n\n💰 Profit sharing\n\n💰 Equity compensation\n\n⬜️ No whiteboard interview\n\n👀 No monitoring system\n\n🚫 No politics at work\n\n🎅 We hire old (and young)\n\n \n\n#Location\nBudapest, Budapest, Hungary
Apply for this job
👉 Please reference you found the job on Remote OK, this helps us get more companies to post here, thanks! |
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Clinical Trial ManagerPrecision for Medicine💰 $118k - $163k* |
ManagerDesignTrainingSupportSoftwareTravelLeadOperationalAnalyticsBiotechHealth |
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Precision for MedicineApply now👀 364 views ✅ 3 applied (1%)
Share this job:
Precision for Medicine is hiring a
Remote Clinical Trial Manager\nWe have current opportunity for an experienced Clinical Trial Manager in Europe! Join our growing team.\n\nPrecision for Medicine is a precision medicine CRO. Precision’s uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs, industry-leading operational and medical experts, advanced biomarker and data analytics solutions, and an unequivocal real passion for rare diseases and oncology, in addition to working across other therapeutic areas.\n\nYou will be the hub of central intelligence for the studies you will be managing, and will lead CRAs and oversee all clinical aspects of your study across multiple countries, ensuring timeline adherence and scope, whilst ensuring quality delivery. We encourage high-energy, dedicated professionals who enjoy a challenge, thrive in the details and flourish in dynamic environments to explore this opportunity. \n\nWe are addressing the challenges facing the research and development of novel compounds in Oncology and are dedicated to positively impacting the health and lives of patients around the world. If you take a consultative approach to trial management, proving to be a valuable partner in the trial operational delivery process, don't miss exploring working with us.\n\nAbout You:\n\n\n* You love having responsibility and a say in how clinical trials are run\n\n* You plan ahead, but have alternative options and a flexible approach\n\n* You are client focused and \n\n* You are well organised and able to manage timelines and shifting priorities, without sacrificing quality.\n\n* You communicate clearly, often and concisely and know that your role is crucial in keeping the trial running smoothly\n\n* You are a master at identifying any risks that threaten projects and handle them resolutely\n\n* You thrive and work with autonomy and ownership to deliver successful outcomes\n\n\n\n\nThe day-to-day role, and how we will support your continued growth:\n\n\n* Management and operational delivery of the clinical elements within a trial including site selection, start-up, enrollment management, site engagement and support, monitoring planning and execution, data cleaning activities and close-out\n\n* Successful execution of assigned trials and ensuring completion of trial deliverables\n\n* Ensure appropriate communication, regulatory documentation, and ongoing oversight of assigned trial(s) by working in close collaboration with other functional team members\n\n* Mentoring and training of team members\n\n* Identify challenges to study timelines/deliverables and offer creative action plans to the team/sponsor\n\n* Lead CRAs as they establish relationships with their sites for high quality oversight of monitoring, regulatory, IP, site payment and overall site correspondence activities\n\n* Maintain team focus on study priorities through efficient cross-functional partnerships and effective communication to achieve the highest level of client satisfaction\n\n\n\n\nQualifications:\n\nMinimum Required:\n\n\n* Bachelor’s degree or equivalent combination of education/experience in science or health-related field, including experience in the field of oncology\n\n\n\n\nOther Required:\n\n\n* Demonstrable experience leading clinical aspects of your studies across multiple countries in a CRO / Pharma or Biotech company (in a dedicated 'clinical lead' role).\n\n* Working knowledge of GCP/ICH guidelines and the clinical development process\n\n* Availability for domestic and international travel including overnight stays\n\n\n\n\nSkills:\n\n\n* Demonstrated computer skills (MS Office, MS Project, PowerPoint) and software experience (CTMS, eTMF, EDC, IXRS)\n\n* Demonstrated ability to develop positive working relationships with internal and external organizations\n\n* Demonstrates core understanding of medical terminology and clinical trial activities as it relates to the execution of a clinical development plan\n\n\n\n\nCompetencies:\n\n\n* Demonstrates mastery knowledge of ICH-GCP, meaningful Precision SOPs, and regulatory guidance, as well as the ability to implement\n\n\n\n\nPrecision medicine is revolutionizing the attack on cancer—and we are passionate about helping you harness its power. We strike tumors on a molecular level using biomarkers to link specific mutations to specific treatments. We combine deep science with deep data from advanced technological platforms, then layer on specialized expertise in the design and execution of targeted, adaptive clinical trials. Ultimately, we deliver robust insights that inform real-time decisions—and optimize the oncology development pathway.\n\n\nAny data provided as a part of this application will be stored in accordance with our Privacy Policy.\n\nPrecision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law. © 2020 Precision Medicine Group, LLC\n\nIf you are an individual with a disability and require a reasonable accommodation to complete any part of the application process, or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at [email protected].\n\n\n \n\n#Salary and compensation\n
No salary data published by company so we estimated salary based on similar jobs related to Design and Travel jobs that are similar:\n\n
$117,500 — $162,500/year\n
\n\n#Benefits\n 💰 401(k)\n\n🌎 Distributed team\n\n⏰ Async\n\n🤓 Vision insurance\n\n🦷 Dental insurance\n\n🚑 Medical insurance\n\n🏖 Unlimited vacation\n\n🏖 Paid time off\n\n📆 4 day workweek\n\n💰 401k matching\n\n🏔 Company retreats\n\n🏬 Coworking budget\n\n📚 Learning budget\n\n💪 Free gym membership\n\n🧘 Mental wellness budget\n\n🖥 Home office budget\n\n🥧 Pay in crypto\n\n🥸 Pseudonymous\n\n💰 Profit sharing\n\n💰 Equity compensation\n\n⬜️ No whiteboard interview\n\n👀 No monitoring system\n\n🚫 No politics at work\n\n🎅 We hire old (and young)\n\n \n\n#Location\nBratislava, Bratislava, Slovakia
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Clinical Trial ManagerPrecision for Medicine💰 $118k - $163k* |
ManagerDesignTrainingSupportSoftwareTravelLeadOperationalAnalyticsBiotechHealth |
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Precision for MedicineApply now👀 416 views ✅ 5 applied (1%)
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Precision for Medicine is hiring a
Remote Clinical Trial Manager\n\n\nWe have current opportunity for an experienced Clinical Trial Manager in Europe! Join our growing team.\n\nPrecision for Medicine is a precision medicine CRO. Precision’s uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs, industry-leading operational and medical experts, advanced biomarker and data analytics solutions, and an unequivocal real passion for rare diseases and oncology, in addition to working across other therapeutic areas.\n\nYou will be the hub of central intelligence for the studies you will be managing, and will lead CRAs and oversee all clinical aspects of your study across multiple countries, ensuring timeline adherence and scope, whilst ensuring quality delivery. We encourage high-energy, dedicated professionals who enjoy a challenge, thrive in the details and flourish in dynamic environments to explore this opportunity. \n\nWe are addressing the challenges facing the research and development of novel compounds in Oncology and are dedicated to positively impacting the health and lives of patients around the world. If you take a consultative approach to trial management, proving to be a valuable partner in the trial operational delivery process, don't miss exploring working with us.\n\nAbout You:\n\n\n* You love having responsibility and a say in how clinical trials are run\n\n* You plan ahead, but have alternative options and a flexible approach\n\n* You are client focused and \n\n* You are well organised and able to manage timelines and shifting priorities, without sacrificing quality.\n\n* You communicate clearly, often and concisely and know that your role is crucial in keeping the trial running smoothly\n\n* You are a master at identifying any risks that threaten projects and handle them resolutely\n\n* You thrive and work with autonomy and ownership to deliver successful outcomes\n\n\n\n\nThe day-to-day role, and how we will support your continued growth:\n\n\n* Management and operational delivery of the clinical elements within a trial including site selection, start-up, enrollment management, site engagement and support, monitoring planning and execution, data cleaning activities and close-out\n\n* Successful execution of assigned trials and ensuring completion of trial deliverables\n\n* Ensure appropriate communication, regulatory documentation, and ongoing oversight of assigned trial(s) by working in close collaboration with other functional team members\n\n* Mentoring and training of team members\n\n* Identify challenges to study timelines/deliverables and offer creative action plans to the team/sponsor\n\n* Lead CRAs as they establish relationships with their sites for high quality oversight of monitoring, regulatory, IP, site payment and overall site correspondence activities\n\n* Maintain team focus on study priorities through efficient cross-functional partnerships and effective communication to achieve the highest level of client satisfaction\n\n\n\n\nQualifications:\n\nMinimum Required:\n\n\n* Bachelor’s degree or equivalent combination of education/experience in science or health-related field, including experience in the field of oncology\n\n\n\n\nOther Required:\n\n\n* Demonstrable experience leading clinical aspects of your studies across multiple countries in a CRO / Pharma or Biotech company (in a dedicated 'clinical lead' role).\n\n* Working knowledge of GCP/ICH guidelines and the clinical development process\n\n* Availability for domestic and international travel including overnight stays\n\n\n\n\nSkills:\n\n\n* Demonstrated computer skills (MS Office, MS Project, PowerPoint) and software experience (CTMS, eTMF, EDC, IXRS)\n\n* Demonstrated ability to develop positive working relationships with internal and external organizations\n\n* Demonstrates core understanding of medical terminology and clinical trial activities as it relates to the execution of a clinical development plan\n\n\n\n\nCompetencies:\n\n\n* Demonstrates mastery knowledge of ICH-GCP, meaningful Precision SOPs, and regulatory guidance, as well as the ability to implement\n\n\n\n\nPrecision medicine is revolutionizing the attack on cancer—and we are passionate about helping you harness its power. We strike tumors on a molecular level using biomarkers to link specific mutations to specific treatments. We combine deep science with deep data from advanced technological platforms, then layer on specialized expertise in the design and execution of targeted, adaptive clinical trials. Ultimately, we deliver robust insights that inform real-time decisions—and optimize the oncology development pathway.\n\n\nAny data provided as a part of this application will be stored in accordance with our Privacy Policy.\n\nPrecision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law. © 2020 Precision Medicine Group, LLC\n\nIf you are an individual with a disability and require a reasonable accommodation to complete any part of the application process, or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at [email protected].\n\n\n \n\n#Salary and compensation\n
No salary data published by company so we estimated salary based on similar jobs related to Design and Travel jobs that are similar:\n\n
$117,500 — $162,500/year\n
\n\n#Benefits\n 💰 401(k)\n\n🌎 Distributed team\n\n⏰ Async\n\n🤓 Vision insurance\n\n🦷 Dental insurance\n\n🚑 Medical insurance\n\n🏖 Unlimited vacation\n\n🏖 Paid time off\n\n📆 4 day workweek\n\n💰 401k matching\n\n🏔 Company retreats\n\n🏬 Coworking budget\n\n📚 Learning budget\n\n💪 Free gym membership\n\n🧘 Mental wellness budget\n\n🖥 Home office budget\n\n🥧 Pay in crypto\n\n🥸 Pseudonymous\n\n💰 Profit sharing\n\n💰 Equity compensation\n\n⬜️ No whiteboard interview\n\n👀 No monitoring system\n\n🚫 No politics at work\n\n🎅 We hire old (and young)\n\n \n\n#Location\nBelgrade, Belgrade, Serbia
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👉 Please reference you found the job on Remote OK, this helps us get more companies to post here, thanks! |
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Clinical Trial ManagerPrecision for Medicine💰 $118k - $163k* |
ManagerDesignTrainingSupportSoftwareTravelLeadOperationalAnalyticsBiotechHealth |
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Precision for MedicineApply now👀 538 views ✅ 8 applied (1%)
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Precision for Medicine is hiring a
Remote Clinical Trial Manager\n\n\nWe have current opportunity for an experienced Clinical Trial Manager in Europe! Join our growing team.\n\nPrecision for Medicine is a precision medicine CRO. Precision’s uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs, industry-leading operational and medical experts, advanced biomarker and data analytics solutions, and an unequivocal real passion for rare diseases and oncology, in addition to working across other therapeutic areas.\n\nYou will be the hub of central intelligence for the studies you will be managing, and will lead CRAs and oversee all clinical aspects of your study across multiple countries, ensuring timeline adherence and scope, whilst ensuring quality delivery. We encourage high-energy, dedicated professionals who enjoy a challenge, thrive in the details and flourish in dynamic environments to explore this opportunity. \n\nWe are addressing the challenges facing the research and development of novel compounds in Oncology and are dedicated to positively impacting the health and lives of patients around the world. If you take a consultative approach to trial management, proving to be a valuable partner in the trial operational delivery process, don't miss exploring working with us.\n\nAbout You:\n\n\n* You love having responsibility and a say in how clinical trials are run\n\n* You plan ahead, but have alternative options and a flexible approach\n\n* You are client focused and \n\n* You are well organised and able to manage timelines and shifting priorities, without sacrificing quality.\n\n* You communicate clearly, often and concisely and know that your role is crucial in keeping the trial running smoothly\n\n* You are a master at identifying any risks that threaten projects and handle them resolutely\n\n* You thrive and work with autonomy and ownership to deliver successful outcomes\n\n\n\n\nThe day-to-day role, and how we will support your continued growth:\n\n\n* Management and operational delivery of the clinical elements within a trial including site selection, start-up, enrollment management, site engagement and support, monitoring planning and execution, data cleaning activities and close-out\n\n* Successful execution of assigned trials and ensuring completion of trial deliverables\n\n* Ensure appropriate communication, regulatory documentation, and ongoing oversight of assigned trial(s) by working in close collaboration with other functional team members\n\n* Mentoring and training of team members\n\n* Identify challenges to study timelines/deliverables and offer creative action plans to the team/sponsor\n\n* Lead CRAs as they establish relationships with their sites for high quality oversight of monitoring, regulatory, IP, site payment and overall site correspondence activities\n\n* Maintain team focus on study priorities through efficient cross-functional partnerships and effective communication to achieve the highest level of client satisfaction\n\n\n\n\nQualifications:\n\nMinimum Required:\n\n\n* Bachelor’s degree or equivalent combination of education/experience in science or health-related field, including experience in the field of oncology\n\n\n\n\nOther Required:\n\n\n* Demonstrable experience leading clinical aspects of your studies across multiple countries in a CRO / Pharma or Biotech company (in a dedicated 'clinical lead' role).\n\n* Working knowledge of GCP/ICH guidelines and the clinical development process\n\n* Availability for domestic and international travel including overnight stays\n\n\n\n\nSkills:\n\n\n* Demonstrated computer skills (MS Office, MS Project, PowerPoint) and software experience (CTMS, eTMF, EDC, IXRS)\n\n* Demonstrated ability to develop positive working relationships with internal and external organizations\n\n* Demonstrates core understanding of medical terminology and clinical trial activities as it relates to the execution of a clinical development plan\n\n\n\n\nCompetencies:\n\n\n* Demonstrates mastery knowledge of ICH-GCP, meaningful Precision SOPs, and regulatory guidance, as well as the ability to implement\n\n\n\n\nPrecision medicine is revolutionizing the attack on cancer—and we are passionate about helping you harness its power. We strike tumors on a molecular level using biomarkers to link specific mutations to specific treatments. We combine deep science with deep data from advanced technological platforms, then layer on specialized expertise in the design and execution of targeted, adaptive clinical trials. Ultimately, we deliver robust insights that inform real-time decisions—and optimize the oncology development pathway.\n\n\nAny data provided as a part of this application will be stored in accordance with our Privacy Policy.\n\nPrecision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law. © 2020 Precision Medicine Group, LLC\n\nIf you are an individual with a disability and require a reasonable accommodation to complete any part of the application process, or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at [email protected].\n\n\n \n\n#Salary and compensation\n
No salary data published by company so we estimated salary based on similar jobs related to Design and Travel jobs that are similar:\n\n
$117,500 — $162,500/year\n
\n\n#Benefits\n 💰 401(k)\n\n🌎 Distributed team\n\n⏰ Async\n\n🤓 Vision insurance\n\n🦷 Dental insurance\n\n🚑 Medical insurance\n\n🏖 Unlimited vacation\n\n🏖 Paid time off\n\n📆 4 day workweek\n\n💰 401k matching\n\n🏔 Company retreats\n\n🏬 Coworking budget\n\n📚 Learning budget\n\n💪 Free gym membership\n\n🧘 Mental wellness budget\n\n🖥 Home office budget\n\n🥧 Pay in crypto\n\n🥸 Pseudonymous\n\n💰 Profit sharing\n\n💰 Equity compensation\n\n⬜️ No whiteboard interview\n\n👀 No monitoring system\n\n🚫 No politics at work\n\n🎅 We hire old (and young)\n\n \n\n#Location\nBucharest, Bucharest, Romania
Apply for this job
👉 Please reference you found the job on Remote OK, this helps us get more companies to post here, thanks! |
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Clinical Research Associate IIPrecision for Medicine💰 $95k - $138k* |
TrainingSupportTravelManagerManagementBiotechHealthHealthcareRecruitmentNon Tech |
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Precision for MedicineApply now👀 991 views ✅ 10 applied (1%)
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Precision for Medicine is hiring a
Remote Clinical Research Associate II\nPosition Summary:\nThe CRA II is a seasoned, experienced professional in monitoring and site management. Responsibilities will be dependent upon the type and timing of the program to which the CRA II is assigned and typically include activities involving start-up and study implementation, on-site monitoring of clinical research studies as well as on-going site management. Incumbents work independently as a study team member.\n\n\nEssential functions of the job include but are not limited to:\n\n\n* Oversees all aspects of study site management to ensure patient safety is protected, quality of data generated by managed sites resulting in consistently low query levels and in acceptable Quality Assurance reports.\n\n* Provides guidance at the site and project level towards audit readiness standards and supports preparation for audit and required follow-up actions.\n\n* Updates, tracks and maintains study specific trial management tools/systems, and status reports.\n\n* If required, manages site start up procedures including the feasibility and recruitment of potential investigators, preparation of EC/IRB submissions, collection and review of regulatory documents, review and adaptation in Patient Informed Consents, notifications to IRB, EC and regulatory authorities, as appropriate, translation of study related documentation, organization of meetings and other tasks as instructed by the Clinical Trial Manager/Project Manager.\n\n* If required, assists the negotiation of study budgets and the execution of investigator contracts under directions of Site Contract Management department/designee.\n\n* Verifies the process of obtaining informed consent has been adequately performed and documented for each subject/patient, as required/appropriate. Assesses factors that might affect subject/patient’s safety and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues.\n\n* Independently conducts all forms of site visits, including pre-study/ qualification, initiation, routine monitoring, and close-out visits, in accordance with the protocol, local laws, ICH-GCP and Precision SOPs. Prepares and submits for review, accurate and timely monitoring reports from all site visits (on-site and remote).\n\n* Documents activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents as per SOPs, Clinical Monitoring Plan/Site Management Plan and client requirements. Supports subject/patient recruitment, retention and awareness strategies. Enters data into tracking systems as required to track all observations, ongoing status and assigned action items to resolution.\n\n* Routinely reviews the Investigator Site File (ISF) for accuracy, timeliness and completeness. Reconciles contents of the ISF with the Trial Master File (TMF). Ensures the investigator/physician site is aware of the requirement of archiving essential documents in accordance with local guidelines and regulations.\n\n* Communicates effectively and proactively with both site personnel and Precision Project and Clinical Trial Management to relay protocol/study issues including any deviations and implements necessary actions in response to those issues.\n\n* Develops and maintains good working relationship with investigators and study staff, serving as an ambassador to promote Precision high quality and professional image.\n\n* Performs investigational product (IP) inventory, reconciliation and reviews storage and security. Verifies the IP has been dispensed and administered to subjects/patients according to the protocol. Verifies issues or risks associated with blinded or randomized information related to IP. Applies knowledge of GCP/local regulations and organizational procedures to ensure IP is appropriately (re)labelled, imported and released/returned.\n\n* Performs data review activities, including remote EDC CRF and patient profiles review, query resolution, and assists data management and clinical data quality personnel to resolve data discrepancies.\n\n* Identifies and processes Serious Adverse Events according to the procedures defined by the study team. Also demonstrates a full understanding of the SAE reporting process.\n\n* Identifies site risks and escalates those to Clinical Trial Manager/Project Manager with suggested contingencies. Owns the timely and appropriate resolution of the risk with minimal support from project team.\n\n* Prepares for and attends Investigator Meetings and/or sponsor face-to-face meetings. Participates in global clinical monitoring/project staff meetings (inclusive of Sponsor representation, as applicable) and attends clinical training sessions according to the project specific requirements.\n\n* Travels as necessary according to project needs.\n\n* Performs other duties as assigned by management.\n\n\n\n\nQualifications:\nMinimum Required:\n\n\n* Europe: University degree life science/pharmacy/other health related discipline or equivalent experience in a scientific or healthcare discipline or be a licensed health care professional.\n\n* N. America: 4-year college degree or equivalent experience in a scientific or healthcare discipline.\n\n* Two (2) years or more as a CRA in either a CRO or pharmaceutical/ biotech industry or equivalent, relevant experience and/or demonstrated competencies. Site management or equivalent experience in clinical research\n\n* One year of oncology monitoring experience\n\n\n\n\nOther Required:\n\n\n* Excellent communication and organizational skills are essential. A team player.\n\n* Evidence of a client focused approach\n\n* Experience using computerized information systems, electronic spreadsheets, word processing and electronic mail.\n\n* Ability to travel overnight. Up to 60% travel on average, based on regional requirements. International travel as needed.\n\n* Fluency in English and for non-English speaking countries the local language of country where position based\n\n\n\n\nPreferred:\n\n\n* Graduate or postgraduate degree\n\n* Oncology phases preferably in early phases\n\n* Experience monitoring in rare and complex therapeutic areas\n\n* Experience monitoring EDC trials and EHR records\n\n* Experience in biopharma or relevant therapeutic area\n\n* Relevant site start-up (feasibility, contract negotiations, submissions) experience for the particular country\n\n* Ability to monitor study sites, with supervision, according to protocol monitoring guidelines, SOPs, GCP and ICH guidelines.\n\n* Ability to resolve project related problems and prioritizes workload to meet deadlines with minimal support from management.\n\n\n\n\nCompetencies:\n\n\n* Exhibits self-motivation and is able to work and plan independently as well as in a team environment\n\n* Understands clinical trials methodology, including a working knowledge of protocols and indications being studied\n\n* Demonstrates professionalism as evidenced by punctuality, ability to deliver on commitments, an understanding of the service culture and positive interactions with customers and teammates, including good interpersonal skills\n\n* Collects data of consistently high standard\n\n* Demonstrated ability to conduct formal presentations to a wide variety of audiences including colleagues, investigative staff, and clients with a high level of proficiency\n\n* Fluency in English and for non-English speaking countries the local language of country where position based\n\n\n \n\n#Salary and compensation\n
No salary data published by company so we estimated salary based on similar jobs related to Travel and Non Tech jobs that are similar:\n\n
$95,000 — $137,500/year\n
\n\n#Benefits\n 💰 401(k)\n\n🌎 Distributed team\n\n⏰ Async\n\n🤓 Vision insurance\n\n🦷 Dental insurance\n\n🚑 Medical insurance\n\n🏖 Unlimited vacation\n\n🏖 Paid time off\n\n📆 4 day workweek\n\n💰 401k matching\n\n🏔 Company retreats\n\n🏬 Coworking budget\n\n📚 Learning budget\n\n💪 Free gym membership\n\n🧘 Mental wellness budget\n\n🖥 Home office budget\n\n🥧 Pay in crypto\n\n🥸 Pseudonymous\n\n💰 Profit sharing\n\n💰 Equity compensation\n\n⬜️ No whiteboard interview\n\n👀 No monitoring system\n\n🚫 No politics at work\n\n🎅 We hire old (and young)\n\n \n\n#Location\nRemote, Oregon, United States
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Proposal ManagerPrecision for Medicine💰 $60k - $100k |
ManagerMicrosoftManagementLeadContent |
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Precision for MedicineApply now👀 563 views ✅ 18 applied (3%)
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Precision for Medicine is hiring a
Remote Proposal Manager\nThe Proposal Manager works closely with a cross-functional team to provide responses to laboratory services RFPs and RFIs from government and commercial clients. The Proposal Manager leads the proposal process from receipt of RFP through internal project scoping and reviews, culminating in final budgets and proposals for submission to the client. Typical duties include leading proposal development meetings, developing pricing for quotes and proposals, writing proposal text, completing RFI responses, and tracking opportunities in Salesforce.com.\n\n \n\nEssential functions of the job include but are not limited to:\n\n\n* Develop strategic proposal responses and budgets in response to RFIs and RFPs\n\n* Lead RFP scoping and proposal review meetings\n\n* Coordinate with various team members to develop content and pricing for simple and complex proposals and quotes\n\n* Perform proposal revisions, as needed\n\n* Maintain current text and template library for use in RFI and RFP responses\n\n* Track proposal status in Salesforce.com from RFP through award\n\n* Work closely with contracts/finance to transition projects after award\n\n\n\n\n \n\nQualifications:\n\nMinimum Required:\n\n\n* Bachelor’s degree or equivalent experience\n\n* 4+ years of related experience\n\n\n\n\n \n\nOther Required:\n\n\n* 4+ years of previous experience in proposals management\n\n* Demonstrated project management experience and ability to multi-task\n\n* Demonstrated ability to develop solutions to complex problems with creativity and innovation\n\n* Must have demonstrated ability to write and edit scientific/technical material\n\n* Exceptional communication skills and the ability to lead proposal development and review meetings\n\n* Proven ability to meet deadlines on multiple projects\n\n* Ability to work cross-functionally with various team members at different levels of the organization\n\n* Strong working knowledge of Microsoft Office programs (Word, Excel, Outlook)\n\n* Must be able to read, write, speak fluently and comprehend the English language\n\n\n\n\n \n\nPreferred:\n\n\n* Bachelor’s in Biology, Business or other relevant discipline\n\n* Laboratory or CRO proposal writing experience preferred\n\n* A solid understanding of laboratory services and processes as they relate to proposal development is highly desirable\n\n* Experience using Salesforce.com for opportunity tracking and reporting is preferred\n\n\n
\n\n#Benefits\n 💰 401(k)\n\n🌎 Distributed team\n\n⏰ Async\n\n🤓 Vision insurance\n\n🦷 Dental insurance\n\n🚑 Medical insurance\n\n🏖 Unlimited vacation\n\n🏖 Paid time off\n\n📆 4 day workweek\n\n💰 401k matching\n\n🏔 Company retreats\n\n🏬 Coworking budget\n\n📚 Learning budget\n\n💪 Free gym membership\n\n🧘 Mental wellness budget\n\n🖥 Home office budget\n\n🥧 Pay in crypto\n\n🥸 Pseudonymous\n\n💰 Profit sharing\n\n💰 Equity compensation\n\n⬜️ No whiteboard interview\n\n👀 No monitoring system\n\n🚫 No politics at work\n\n🎅 We hire old (and young)\n\n \n\n#Location\nRemote, Oregon, United States
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Regulatory and Start Up SpecialistPrecision for Medicine💰 $30k - $50k* |
SupportTravelManagementLeadBiotechHealthcareNon Tech |
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Precision for MedicineApply now👀 1,331 views ✅ 86 applied (6%)
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Precision for Medicine is hiring a
Remote Regulatory and Start Up Specialist\n \n\nPosition Summary: \n\nThe Regulatory and Start Up Specialist (RSS) is an experienced professional in regulatory and site start-up activities. Responsibilities will be dependent upon the location of the RSS and include but are not limited to initial and subsequent clinical trial submission to Competent Authorities and IRB/ Ethics Committees, Informed Consent Form review and adaptation, Essential Document collection and quality review, supporting sites on IRB/EC submissions and provide support to the Site Contract Management group in budget and contract negotiation. The RSS may act as Subject Matter Expert for questions by other in-country members (CRAs, CSSs or others) supporting site start-up activities and may contribute to development or revision of country specific tools and guidance documents to ensure compliance with local and international clinical trials regulations and guidelines. \n\nThis is a remote position and employee must reside in Canada.\n\nEssential functions of the job include but are not limited to: \n\n\nResponsible for delivery, in terms of timeliness and quality, of site activation readiness within the assigned country/sites and foreseeing and mitigating any risks. \n\nPreparation of Clinical Trial Application Forms as well as preparation of submission dossier (initial and amendments/notifications) for submission to CA, EC, and other applicable local bodies according to local requirements and within required timelines to obtain all necessary authorizations/approvals for the conduct of the Clinical Trial according to international and local/national applicable regulations, company SOPs and principles of ICH-GCP. \n\nInteraction with CA/EC for study purposes and handling responses to the CA/EC. \n\nProviding regular updates about CA and EC submissions to the Start Up Lead and/or Regulatory Lead assigned to the study and to Project Manager/Project Team as relevant. \n\nMaintenance of project plans, project trackers and regulatory intelligence tools as it pertains to assigned responsibilities and to keep Regulatory Leadership updated. \n\nPreparation/Support the development of study specific start-up plans, IMP release requirements and essential document review criteria. \n\nPartner with the assigned site CRA to ensure alignment in communication and secure site collaboration. \n\nPrepare. review and manage collection of essential documents required for site activation/IMP release. \n\nCustomize country/site specific Patient Information Sheet and Informed Consent Forms. \n\nResponsible for/facilitates the translation and co-ordination of translations for documents required for submission. \n\nMaintain communication with other key functions participating to country start up i.e., Feasibility, Clinical Operations, Project Management, Regulatory, and Site Contracts management group on project specific status and deliverables. \n\nAct as SME for collection and maintenance of site level critical path to Site Activation data points, including but not limited to Competent Authority, local IRB/Ethics Committee (EC) timelines, site contracts and budget negotiation requirements for and other required reviews to secure on time site activation for the assigned sites in the country. \n\nWhen required, participate/support the negotiation of study budgets and the execution of investigator contracts under directions of Site Contract Management department/designee department. \n\nMay participate/support feasibility group in site outreach to assess potential interest of investigators to a potential study. \n\nKeep an updated knowledge of the local clinical trial laws, regulations and help distributing their knowledge within PfM to ensure the conduct of Clinical Trials according to international and local/national applicable regulations. \n\nMaintain audit/inspection readiness at all times and file documents as per TMF plan and/ or study specific plans in the relevant TMF \n\nMay support the clinical team performing Pre-Study Site Visits. \n\nMay support process improvement initiatives, training, and mentoring. \n\nPerforms other duties as assigned by management. \n\n\n\n\nQualifications: \n\nMinimum Required: \n\n\n* Fluent in English and French\n\nBachelor’s degree in life sciences or related field (ideally in a scientific or healthcare discipline), or Registered Nurse (RN) or equivalent combination of education, training, and experience. \n\n1 year or more as a Regulatory or SU specialist (or comparable role) in either a CRO or pharmaceutical/ biotech industry or equivalent, relevant experience and/or demonstrated competencies \n\n\n\n\nOther Required: \n\n\nStrong communication and organizational skills are essential. \n\nExperience using computerized information systems, electronic spreadsheets, word processing and electronic mail required. \n\nFluency in English and for non-English speaking countries the local language of country where position based. \n\n\n\n\nPreferred: \n\n\nRelevant regulatory and site start-up (feasibility, contract negotiations, CA/ EC/ IRB submissions) experience for the particular country. \n\nExperience using milestone tracking tools/systems. \n\nAbility to prioritize workload to meet deadlines. \n\nAdvanced degree in medical or life sciences (MD, PhD, PharmD)/RAC certification/Masters in Regulatory Science \n\n\n\n\nCompetencies \n\n\nKnowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements. \n\nAbility to follow task-specific procedures, be attentive to detail and place importance on accuracy of information. \n\nStrong organizational skills. \n\nAbility to effectively interact with project team(s) and effectively communicate in English and the local language of the country where located. \n\nAbility to work independently in a fast-paced environment with a sense of urgency to match the pace. \n\nMust demonstrate excellent computer skills. \n\nGood communication, presentation, interpersonal skills, both written and spoken, with an aptitude to learn how to inform, influence, convince, and persuade. \n\nFlexible attitude with respect to work assignments, and new learning. \n\nOccasional travel may be required. \n\n\n\n\n#LI-REMOTE\n\n \n\n#Salary and compensation\n
No salary data published by company so we estimated salary based on similar jobs related to Non Tech and Non Tech jobs that are similar:\n\n
$30,000 — $50,000/year\n
\n\n#Benefits\n 💰 401(k)\n\n🌎 Distributed team\n\n⏰ Async\n\n🤓 Vision insurance\n\n🦷 Dental insurance\n\n🚑 Medical insurance\n\n🏖 Unlimited vacation\n\n🏖 Paid time off\n\n📆 4 day workweek\n\n💰 401k matching\n\n🏔 Company retreats\n\n🏬 Coworking budget\n\n📚 Learning budget\n\n💪 Free gym membership\n\n🧘 Mental wellness budget\n\n🖥 Home office budget\n\n🥧 Pay in crypto\n\n🥸 Pseudonymous\n\n💰 Profit sharing\n\n💰 Equity compensation\n\n⬜️ No whiteboard interview\n\n👀 No monitoring system\n\n🚫 No politics at work\n\n🎅 We hire old (and young)\n\n \n\n#Location\nMontreal, Quebec, Canada
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👉 Please reference you found the job on Remote OK, this helps us get more companies to post here, thanks! |
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CTMS System SpecialistPrecision for Medicine 💰 $60k - $120k* |
SystemDesignTrainingTechnicalSupportTestManagerAdministratorManagementLeadOperationsOperationalAnalyticsHealthFull-Time |
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Precision for MedicineApply now👀 816 views ✅ 1,244 applied (152%)
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Remote CTMS System SpecialistCTMS System Specialist\nWe have current opportunities for a CTMS System Specialist in Europe! Join our growing team.\nPrecision for Medicine is a precision medicine CRO. Precision’s uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs, industry-leading operational and medical experts, advanced biomarker and data analytics solutions, and an unequivocal real passion for rare diseases and oncology, in addition to working across other therapeutic areas.\nWe offer flexible location options, and remote based working. This position can be based in one of the following countries: UK, France, Spain, Italy, Germany, Belgium, Netherlands, Poland, Hungary, Serbia. Romania, Slovakia. \nPosition Summary:\nWe are seeking a responsible, dynamic, creative and highly motivated CTMS System Specialist to join our Clinical Operations Department. This full-time position will serve as a subject matter expert over CTMS, supports the Clinical Study team in the set-up and configuration of the system, as well as ongoing maintenance of the system for studies lifecycle. This position will collaborate with Clinical Systems Manager and IT to define and deliver solutions that successfully meet the above objectives. This position will collaborate with Clinical Systems leadership and IT to define and deliver solutions that successfully meet the above objectives. Responsible for combining clinical operations and technology skills with excellent independent work ethic, communication, facilitation, and presentation skills. Provides technical guidance and support with respect to the CTMS and other systems. \n \nEssential functions of the job include but are not limited to:\n\nProvide advanced System Administrator management of Precision’s Clinical Trial Systems, serving as main subject matter expert (SME) for the CTMS and eTMF system.\n\nAssist with new version releases and configuration changes, including development, testing, and validation oversight or as needed User Acceptance Test (UAT) execution.\n\nCollaborate with study team leads to lead the set-up of studies, study teams and sites in the CTMS ensuring programs are configured according to the specific study requirements including: countries and sites; grant access for internal, sponsor and 3rd party vendor users; baseline expected deviation categories, study/visit plans, visit report & letter templates and baseline milestones\n\nWork with data management and clinical programming to establish potential for integration with EDC.\n\nManage end-user and group permission settings.\n\nProvide adequate training of system functionality to study teams, including external partners, sponsor and/or site staff, to ensure that study teams have the guidance needed to work CTMS features independently and meet periodically with study teams to offer ongoing support.\n\nCreate and/or provide input for the creation of work instructions/job aids, assess global & project specific trip report & letter templates, assist teams with workflows and provide training materials/tools as needed.\n\nContinually assess that CTMS features are functioning properly and efficiently; track all issues & observations for future enhancement, bug fixes, or ongoing needs for training of CTMS features for continuous improvement of the management of the system.\n\nIntegrate CTMS activities in line with integrations with the corresponding eTMF as necessary.\n\nClinical Trial Management duties (as needed):\n\n\nCreate and manage study timelines and milestones.\n\nAssist with the site status.\n\nAssess subject enrollment, status, visit dates, procedures, etc.\n\nEntry of monitoring visits, study activities, deviations, assist with trip report workflows, develop activity plans, etc.\n\nMonitor completeness and quality of the CTMS (from start up to final deliverable). \n\nPerform periodic reviews to ensure CTMS adoption and progress is timely and in line with the current stage of each program.\n\n\n\n\n\nQualifications:\nMinimum Required:\n\nBachelor’s Degree preferred.\n\n4+ years of Clinical Systems team experience within a CRO is highly preferred.\n\n\n\nOther Required:\n\n2+ years CTMS or other clinical program management system(s) experience\n\nWorking knowledge of ICH-GCP guidelines and major Health Authority regulations as they pertain to the operational aspects of clinical studies and the management of TMF content.\n\nExcellent planning, organizational and time management skills, including the ability to support and prioritize multiple projects.\n\nExtensive knowledge of monitoring and site management; some knowledge of study management and reporting needs.\n\nProven ability to collaborate in a team environment and work independently\n\nExcellent oral and written communication skills\n\n\n\nPreferred:\n\n\nWorking knowledge of and experience with Medidata Rave CTMS\n\nWorking knowledge of and experience with TransPerfect Trial Interactive eTMF\n\nProficient in MS Excel\n\nSome experience with Adobe Acrobat, creation and development of editable/fillable Adobe forms\n\nMS project or other GANTT charting and milestone development is a plus\n\nMust be a team-player, punctual and reliable, dependable and flexible in adapting to change in a multi-disciplinary, fast-paced work environment\n\n\n\n\nPrecision medicine is revolutionizing the attack on cancer—and we are passionate about helping you harness its power. We strike tumors on a molecular level using biomarkers to link specific mutations to specific treatments. We combine deep science with deep data from advanced technological platforms, then layer on specialized expertise in the design and execution of targeted, adaptive clinical trials. Ultimately, we deliver robust insights that inform real-time decisions—and optimize the oncology development pathway.\n\n\nAny data provided as a part of this application will be stored in accordance with our Privacy Policy.\n\nPrecision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law. © 2020 Precision Medicine Group, LLC\n\nIf you are an individual with a disability and require a reasonable accommodation to complete any part of the application process, or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at [email protected].\n \n\n#Salary and compensation\n
No salary data published by company so we estimated salary based on similar jobs related to Design, Support and Digital Nomad jobs that are similar:\n\n
$60,000 — $120,000/year\n
\n\n#Benefits\n 💰 401(k)\n\n🌎 Distributed team\n\n⏰ Async\n\n🤓 Vision insurance\n\n🦷 Dental insurance\n\n🚑 Medical insurance\n\n🏖 Unlimited vacation\n\n🏖 Paid time off\n\n📆 4 day workweek\n\n💰 401k matching\n\n🏔 Company retreats\n\n🏬 Coworking budget\n\n📚 Learning budget\n\n💪 Free gym membership\n\n🧘 Mental wellness budget\n\n🖥 Home office budget\n\n🥧 Pay in crypto\n\n🥸 Pseudonymous\n\n💰 Profit sharing\n\n💰 Equity compensation\n\n⬜️ No whiteboard interview\n\n👀 No monitoring system\n\n🚫 No politics at work\n\n🎅 We hire old (and young)\n\n \n\n#Location\nBelgrade, Belgrade, Serbia
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Senior Clinical Data ManagerPrecision for Medicine 💰 $60k - $120k* |
ManagerDesignTestingMicrosoftManagementSeniorHealthHealthcare |
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Precision for MedicineApply now👀 1,416 views ✅ 1,233 applied (87%)
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Precision for Medicine is hiring a
Remote Senior Clinical Data Manager\nWhy consider joining us? As a member of our thriving team, you have the opportunity to work alongside clinical research colleagues who understand the patients’ mindset and their disease experiences. We help translate science into success for trials with a strategic and targeted, patient-centric approach. We are specialists who find solutions for novel trial challenges in our detailed approach throughout every study phase. From the beginning, we have nurtured an employee-centric company culture that focuses on patients’ needs. Precision’s team-focused culture ensures that team members will thrive and learn. These important key elements result in high quality work output while still having fun and giving back to the patient community. \n\nAbout You:\n\n\n* Want to do a good job, help others and have a passion for making a difference.\n\n* Care about patients and understand the importance of quality data leading to successful outcomes.\n\n* Are highly experienced in clinical data management and have keen attention to detail, clear communication abilities and organizational skills.\n\n* Foster and value client and internal team collaboration.\n\n* Have a strong belief that all team members are valuable and appreciated.\n\n* Enjoy working alongside teammates and having project-specific data management and managerial support.\n\n* Excited about exercising your data management knowledge and expertise.\n\n* Look forward to opportunities to be involved in innovative data management technology initiatives and training.\n\n\n\n\n A glimpse into the day to day:\n\n\n* Lead all aspects of the clinical trial data management process from pre-study start up to post database lock for assigned projects. \n\n* Collaborate with clients and team members to develop Case Report Forms (CRFs) and methodical data cleaning strategies to support protocol endpoints.\n\n* Be involved in the Electronic Data Capture (EDC) clinical database development and user acceptance testing (UAT).\n\n* Actively cleaning data, managing CRF and query trends and data reporting to ensure a clean database lock ready for analysis.\n\n* Work alongside key functional areas (such as Project Management, Biostatistics, Medical, Clinical, Safety, Quality Assurance, etc.).\n\n* Standard Operating Procedures / Work Flow Tools (SOPs/WFTs); regulatory directives; study specific plans and guidelines will be followed.\n\n\n\n\nQualifications:\n\nMinimum Required: Bachelor’s degree or in country local equivalent or equivalent related experience\n\nOther Required:\n\n\n* Minimum 5 years of Clinical Data Management experience utilizing various clinical database management systems\n\n* Broad knowledge of drug, device and/or biologic development and effective data management practices\n\n* Proficiency in Microsoft Office: Word, Excel, PowerPoint, Outlook\n\n* Excellent organizational, interpersonal & leadership skills\n\n* Professional use of the English language; both written and oral\n\n\n\n\nPreferred:\n\n\n* Experience in a clinical, scientific or healthcare discipline. Understanding of CDISC standards (CDASH, SDTM, etc.). \n\n* Academic concentration in one or more of the following, or related discipline; life sciences, computer science, or engineering.\n\n* Advanced degree in clinical data management, health informatics, biometrics or similar.\n\n\n\n\nPrecision medicine is revolutionizing the attack on cancer and rare diseases—and we are passionate about helping you harness its power. We strike tumors on a molecular level using biomarkers to link specific mutations to specific treatments. We combine deep science with deep data from advanced technological platforms, then layer on specialized expertise in the design and execution of targeted, adaptive clinical trials. Ultimately, we deliver robust insights that inform real-time decisions—and optimize the oncology development pathway. \n\n#Salary and compensation\n
No salary data published by company so we estimated salary based on similar jobs related to Design, Testing, Microsoft, Senior and Digital Nomad jobs that are similar:\n\n
$60,000 — $120,000/year\n
\n\n#Benefits\n 💰 401(k)\n\n🌎 Distributed team\n\n⏰ Async\n\n🤓 Vision insurance\n\n🦷 Dental insurance\n\n🚑 Medical insurance\n\n🏖 Unlimited vacation\n\n🏖 Paid time off\n\n📆 4 day workweek\n\n💰 401k matching\n\n🏔 Company retreats\n\n🏬 Coworking budget\n\n📚 Learning budget\n\n💪 Free gym membership\n\n🧘 Mental wellness budget\n\n🖥 Home office budget\n\n🥧 Pay in crypto\n\n🥸 Pseudonymous\n\n💰 Profit sharing\n\n💰 Equity compensation\n\n⬜️ No whiteboard interview\n\n👀 No monitoring system\n\n🚫 No politics at work\n\n🎅 We hire old (and young)\n\n \n\n#Location\nGladstone, New Jersey, United States
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Project Manager Senior Project ManagerPrecision for Medicine 💰 $70k - $120k* |
ManagerSoftwareTravelFinancialEduCManagementLeadSeniorOperationalAnalyticsLegalBiotechHealth |
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Precision for MedicineApply now👀 1,728 views ✅ 1,251 applied (72%)
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Precision for Medicine is hiring a
Remote Project Manager Senior Project Manager\nAre you an experienced full service Project Manager in the field of clinical trials who’s engaged in addressing the challenges facing the research and development of novel compounds in Oncology, Rare Disease or CNS? Are you passionate about impacting the health and lives of patients around the world? Do you take a consultative approach to trial management, proving to be a valuable partner in trial operational delivery?\n\nPrecision for Medicine (CRO) are looking for experienced Project Managers ideally with experience in ONCOLOGY and/or RARE DISEASES or CNS who have managed full service clinical trials within a CRO/Pharmaceutical setting. \n\nWe can offer a Project Manager or Senior Project Manager position depending on level of experience. We are flexible to consider any European location where PFM have a legal entity, including: UK, Spain, France, Germany, Italy, Poland, Hungary, Romania, Slovakia, Serbia, Belgium, Netherlands or in Australia. \n\nIn this pivotal role you will have full service oversight for clinical projects across global/regional (ph I-IV) trials, within Oncology (or Rare Diseases or CNS). Accountable for clinical project delivery, oversight of all functional departments, and ensuring agreed timelines, scope, cost and quality.\n\nInvolved in all study stages, including proposal strategy, development, costing, and bid defence, and seeing studies through the full cycle to completion, managing the client relationship, project team and budget and timelines throughout.\n\nYou will work in a cross-functional team with both internal and external stakeholders, driving quality and coordinating the study team.\n\nPrecision for Medicine is a precision medicine CRO. Our uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs, industry-leading operational and medical authorities, advanced biomarker and data analytics solutions, and an unequivocal real passion for rare diseases and oncology.\n\nWe are a people focussed CRO with a supportive and collaborative environment which promotes work life balance and encourages team development. \n\nWe invite you to learn more about our growing organization serving our clients that are researching ground-breaking cancer therapies. We strive to ensure employees feel appreciated for the contributions they make every single day.\n\nWe offer an amazing high-energy, dedicated, collaborative team members who enjoy a challenge, thrive in the details and flourish in dynamic environments. If you are no stranger to taking charge and seek positive teamwork to deliver extraordinary work, we have an opportunity for you.\n\nHow we will keep you busy and support your growth:\n\n\n* You will independently lead clinical projects in accordance with the study budget and scope of work. You will use your strong interpersonal and organizational skills to set and achieve objectives in the execution of the projects; both contracted objectives and financial objectives. You may be called upon to run international trials as well.\n\n* Serve as the primary point-of-contact liaison with the client to provide excellent customer service, including participation in proposal activities and client presentations\n\n* Liaise with Project Team and senior management of both Precision and sponsors, including C level\n\n* Handle and lead all aspects of a clinical research trial or trials\n\n* Total project management for all functional areas including data management, safety, clinical, medical monitoring and biostatistics, etc.\n\n* Prepare project status updates for clients and management; identifying key deliverables and performance metrics of success and escalation.\n\n* Serve as an active member of the Project Team with the goal to contribute towards efficient management and execution of trials\n\n* Prepare and reviews protocols and other study documentation such as project plans, inform consents, site contracts and budgets\n\n\n\n\nRequirements:\n\n\n* Degree or similar related life science qualification, or equivalent combination of education and experience.\n\n* Previous experience in a full service/global Project Management role is essential.\n\n* 5 to 7 years industry experience and at least 3 years full service Project Management experience in a clinical trial setting working for a CRO, pharmaceutical or biotech company.\n\n* Working understanding of GCP/ICH guidelines and the clinical development process\n\n* Ability to drive and availability for domestic and international travel including overnight stays\n\n* Proven computer skills (MS Office, MS Project, PowerPoint) and software experience (CTMS, eTMF, EDC, IXRS)\n\n* Proven ability to develop positive working relationships with individual and teams internally and externally\n\n* Demonstrated core understanding of medical terminology and clinical trial activities as it relates to the execution of a clinical development plan\n\n\n\n\n#LI-NC1 #LI-Remote \n\n#Salary and compensation\n
No salary data published by company so we estimated salary based on similar jobs related to Travel, Education, C, Senior, Legal and Biotech jobs that are similar:\n\n
$70,000 — $120,000/year\n
\n\n#Benefits\n 💰 401(k)\n\n🌎 Distributed team\n\n⏰ Async\n\n🤓 Vision insurance\n\n🦷 Dental insurance\n\n🚑 Medical insurance\n\n🏖 Unlimited vacation\n\n🏖 Paid time off\n\n📆 4 day workweek\n\n💰 401k matching\n\n🏔 Company retreats\n\n🏬 Coworking budget\n\n📚 Learning budget\n\n💪 Free gym membership\n\n🧘 Mental wellness budget\n\n🖥 Home office budget\n\n🥧 Pay in crypto\n\n🥸 Pseudonymous\n\n💰 Profit sharing\n\n💰 Equity compensation\n\n⬜️ No whiteboard interview\n\n👀 No monitoring system\n\n🚫 No politics at work\n\n🎅 We hire old (and young)\n\n \n\n#Location\nBrussels, Brussels-Capital, Belgium
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