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Thus, the candidate should also have an understanding of various clinical trial activities such as Clinical Trial Management Services, clinical monitoring, data management, Real World Data/Evidence (RWD/RWE), biostatistics, medical writing, Ph 1 CRU, central lab, biomarker lab, bioanalytical lab, RTSM, eCOA, medical imaging, safety, e-informed consent, mobile HCP services, telemedicine and wearables/sensors.
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We seek a Cancer Clinical Research Coordinator Associate to help us enact our mission to reduce cancer mortality through comprehensive programs of cancer research, treatment, education, and outreach.
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A Clinical Trials Management Associate - III. Clinical Trials Management Associate - III. Meets all requirements for Clinical Trial Management Associate (CTMA) grade 25 position with demonstrable proficiency.
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Assists Biomarker Sciences, Clinical Virology, and/or Clinical Pharmacology in vendor selection and coordinates all interactions and deliverables from vendors. Clinical Operations - Biomarker and Bioanalytical Operations.
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Duration: 6 monthsLocation: Foster City, CAAs a Clinical Trials Management Associate - III, you will:Job Description:Function: Clinical Operations - Biomarker and Bioanalytical OperationsPosition Overview:Clinical Operations is responsible for the worldwide execution of all Phase I - IV clinical trials across all clients therapeutic areas.
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Title : Sr. Clinical Trial Management Associate (Senior CTMA) Location : Foster City California 94404 United States (Need local ) Pay :$62/hr. on W2 Only FUNCTION: Clinical Operations - Biomarker and Bioanalytical Operations Qualifications Job Description: POSITION OVERVIEW: Clinical Operations is responsible for the worldwide execution of all Phase I - IV clinical trials across all company therapeutic areas.
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JOB TITLE: Sr. Clinical Trial Management Associate (Senior CTMA) FUNCTION: Clinical Operations Biomarker and Bioanalytical Operations. Clinical Operations plays a key role in ensuring all Gilead clinical trials are performed in accordance with applicable SOPs, company policies and regulatory guidelines to provide timely and high-quality clinical data that supports global registration and commercialization of Gileads products.
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Summary: Plan and coordinate all operat Clinical, Management, Associate, Clinic, Healthcare, Staffing. Our Bay Area pharmaceutical client is recruiting for a Sr Clinical Trial Management Associate with biosample management experience to join their growing team.
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Job ID: 24-03484 JOB TITLE: Sr. Clinical Trial Management Associate (Senior CTMA) Participates in the functional review of study protocol and other study related documents such as clinical sample management plan, study communication plan, or presentations for Investigator and/or Study Kick-Off meeting.
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The Associate Director (AD) Clinical Study Management leads both indirect and direct reports, external partners, consultants, vendors and external budget to ensure the timely and cost-effective implementation of clinical trials.
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Innova Solutions is immediately hiring Manager Vendor OutsourcingPosition type: Fulltime – Contract Duration: 12 MonthsLocation: REMOTE As Manager Vendor Outsourcing, you will: Job Description: The R&D Sourcing and Contracting Associate will be responsible for assistance in the pre-clinical / research, clinical sourcing in support of Client’s global Phase I-IV clinical trials, and other ad hoc projects in the Vendor Outsourcing department.
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Clinical operations/bioanalytical operations experience, laboratory (bench) experience. Complete knowledge of Food & Drug Administration (FDA) and European Medicines Agency (EMA), and other applicable national regulations, International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) guidelines, Good Clinical Practice (GCP) and key Clinical Operations principles, concepts, practices, standards, processes and tools.
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Has excellent communication skills and is comfortable interacting with internal and external teams, such as, clinical operations, finance, legal, business conduct, vendor management and payments.
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Natera is currently seeking a Clinical Laboratory Associate 1 to analyze laboratory specimens following the standard methods and procedures while. Natera is currently seeking a Clinical Laboratory Associate 1 to analyze laboratory specimens following the standard methods and procedures while.
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Work with vendors to ensure that all study services comply with the study plan and budget; this may include clinical research organizations (CROs), electronic data capture vendors (EDC), and suppliers.
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Title: clinical associate in Half Moon Bay, CA
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