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๐Ÿข Precision for Medicine Remove this filter
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Precision for Medicine


๐Ÿ‡บ๐Ÿ‡ธ United States
๐Ÿ’ฐ $60k - $120k*

Manager

 

Design

 

Testing

Microsoft

Management

Senior

Health

Healthcare

Precision for Medicine

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๐Ÿ‘€ 83 views

โœ… 4 applied (5%)

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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 patientsโ€™ 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 patientsโ€™ needs. Precisionโ€™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: Bachelorโ€™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 diseasesโ€”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 decisionsโ€”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#Location\nGladstone, New Jersey, United States
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Precision for Medicine


๐Ÿ‡ง๐Ÿ‡ช Belgium
๐Ÿ’ฐ $70k - $120k*

Manager

 

Software

 

Travel

Financial

Edu

C

Management

Lead

Senior

Operational

Analytics

Legal

Biotech

Health

Precision for Medicine

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๐Ÿ‘€ 356 views

โœ… 20 applied (6%)

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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 whoโ€™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#Location\nBrussels, Brussels-Capital, Belgium
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