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A scientific degree with directly relevant professional experience in small molecule product development, global CMC regulatory affairs, and CMC technical areas of at least 12 years with a BA/BS or 10 years with an MA/MS, PhD, PharmD, or MD.
$307,560Full-timeExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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Collaborate with cross-functional teams including biostatisticians, project management, clinical data managers, scientific affairs, medical affairs, and regulatory affairs to ensure timely and accurate delivery of statistical programming deliverables.
$174,182 a yearFull-timeExpandApply NowActive JobUpdated 27 days ago - UpvoteDownvoteShare Job
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PharmD or PhD in clinical research or clinical pharmacology with 8+ years' scientific and/or drug development experience in the biopharma industry, healthcare, consulting, academia or a related environment.
$307,560 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Provide PV leadership for Jazz Pharmaceuticals Clinical Development including Clinical, Investigator Sponsored, Compassionate Use, and Disease Monitoring Programs; liaise with Clinical Sciences, Clinical Operations, Medical Affairs, Biometrics, Regulatory Affairs, Contract Research Organizations (CROs), Data Monitoring Committees (DMCs) and other entities to contribute to overall study execution while ensuring safety strategy and operational excellence.
$420,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Oversee Gilead’s investigator sponsored research program in HIV prevention, including determining ISR funding priorities in line with Phase 4 integrated evidence plans (IEPs), oversight of RFP development and execution, and working with Gilead’s clinical operations team to manage the ISR portfolio.
Full-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Initiates and executes pre-clinical scientific research and development in the Molecular Biology Research team. Plans and executes laboratory research. Focuses on advancing Natera’s oncology portfolio and works within a research team inventing and evaluating new technologies for applications in oncology, NIPT, and transplant assessment.
Full-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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CMC Regulatory Affairs, oncology, small molecule, drug development, clinical development. Director, CMC Regulatory Affairs. 15+ years of pharmaceutical/biotech drug development experience with 5+ years of experience in global CMC regulatory affairs with working experience and content knowledge in CMC development of NCEs/small molecules.
Full-timeExpandApply NowActive JobUpdated 26 days ago - UpvoteDownvoteShare Job
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Building on CARGO’s preclinical and clinical experience, the Discovery Research team at CARGO aims to evaluate and implement cutting edge technologies to deliver optimally functional T cells to a larger number of patients.
$141,000 a yearFull-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Stanford Synchrotron Radiation Lightsource (SSRL), a SLAC Directorate at Stanford University, is a national scientific user facility providing synchrotron radiation for research in biology, chemistry, engineering, environmental science, material science, medicine, and physics.
$163,000 a yearFull-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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BA/BS Degree in Business, Life Sciences, Paralegal with a minimum of 3 years of independent study start-up/feasibility experience in clinical research or 10 + years of direct experience. Work closely with clinical operations, regulatory affairs, and other departments to ensure smooth study start-up processes.
$70 an hourFull-timeExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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R&D Partners is a national staffing firm focused in the areas of: Scientific, Clinical Research and Engineering. Biotechnology company is hiring a Research Associate II within the Pathobiology department to contribute to histology and pathology workflows in support of pre-clinical in vivo pharmacology studies.
Full-timeExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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Possesses a passion for being part of the scientific and engineering community, helping bring cutting edge research to enable commercial processes. Codexis, a biotechnology company based in Redwood City, CA, is looking to hire a Research Associate III – Protein Engineering.
$107,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The primary duty of the Clinical Research Assistant - Assistant Fitness Instructor will be the implementation of a virtually delivered group exercise program for Spanish-speaking persons who are waiting for a kidney transplant.
$30 an hourFull-timeExpandApply NowActive JobUpdated 27 days ago - UpvoteDownvoteShare Job
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The work will be conducted in a highly interactive and collaborative multi-disciplinary scientific environment. Plans and executes experiments that support research activities and project goals.
Full-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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JOB SUMMARYThe Research RN, NCHRI works directly with the physician in accurately and professionally executing all clinical research projects in an acute care/inpatient setting (ED, Cath Lab, ICU, EP lab, Step down and OR) as well as the ambulatory and ancillary areas.
$10,000 a yearFull-timeExpandApply NowActive JobUpdated Today
clinical research scientific affairs jobs Title: director Company: Biophase in Foster City, CA
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