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Thorough knowledge of clinical research concepts, practices, and FDA regulations and ICF Guidelines regarding drug development phases, clinical research, and data management methods.
$80,000 - $100,000 a yearExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Experience with IRB administration and data management is required. The Project Manager will plan and implement study protocols, create standard operating procedures, collect, and manage study data, assist in study outreach and engagement activities, perform systematic literature reviews, and synthesize relevant data.
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Basic understanding of clinical and biomedical research, GCP, GLP, CLIA, data management, risk management and regulatory issues. The Project Manager - Biospecimen will be an independent contributor who will work closely with Clinical Teams to develop and implement biospecimen management plan for client-sponsored Phase 1-4 clinical trials and externally acquired biospecimens.
Full-timeExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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You will work with experienced project representatives, subject matter expert scientists, and the clinical trials teams including clinical operations, data management, and business operations functions to implement and maintain validated bioanalytical assays at third-party laboratory vendors.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Ensure through study team management that the necessary regulatory, safety and data evaluation requirements are met to allow the conduct of clinical related activities in conjunction with the Regulatory, Pharmacovigilance (GPS), Data Management and Statistics Departments.
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Senior Project Manager, Global Clinical Drug Supply - Strategy & Innovation will work in partnership with several internal and external stakeholders, including GCDS Operations, GCDS Systems, Development Operations, Research & Development Strategic Initiatives, Portfolio & Project Management, and CMC.
$190,625 a yearFull-timeExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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Act as the primary point of contact for cross-functional teams, including clinical operations, regulatory affairs, pharmacovigilance, and data management. 5+ years of experience in clinical project management within the biotech, pharmaceutical, or CRO industry, preferably within early-phase studies.
$220,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Project Team Performance Identify, assign, and monitor the completion of interdisciplinary project tasks that include site monitoring, CRF and database development and revision, data collection, patient safety/adverse event management, document management, statistical analysis, and/or final report writing and publications.
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Independently manage interactions with clinical monitors, data management, safety, regulatory, pharmaceutical science and QA team members, both internally and externally. The CPM will be responsible for all aspects of clinical trial management aimed at treating a rare or infectious liver-targeted disease.
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Lead sample management for the clinical study beginning with oversight of shipment conditions and timing from the clinical site to the central laboratory, delivery of samples to the bio-analytical vendor, testing, reconciliation, data transfer, and final long-term storage or further use approval of clinical samples.
$170,500 a yearFull-timeExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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Experience in handling integration management, process and continuous improvement management, digital or data technology, operations, supply chain, manufacturing, ERP, clinical supply chain, logistics, preferably in the pharmaceutical or biopharmaceutical industry.
$190,625 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The Sr. Clinical Project Manager is responsible for the overall execution and management of their assigned projects, from initial study start-up to study close/database lock.
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Provide strategic input into study documents such as study synopsis, protocol, ICF, CRFs, CRF Completion Guidelines, Study Execution Plans, Clinical Data Review Plan, Safety Plan, Clinical Database edit specifications, Annotated Monitoring Visit Report templates, Clinical Study Report development, etc.
Full-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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Collaborate with medical research, data management, biostatistics, pharmacovigilance, and other functions to ensure data is processed in a timely manner for ongoing data review, interim analyses and final database lock.
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3+ years of professional experience in a project management role, including 1+ years of work experience in the life science or healthcare industry and familiarity with project management methodologies and tools.
Full-timeExpandApply NowActive JobUpdated Today
data management jobs Title: project manager clinical
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