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Duration: 6 months Location: Foster City, CA As a Clinical Trials Management Associate - III, you will: Job Description: Function: Clinical Operations - Biomarker and Bioanalytical Operations Position 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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Innova Solutions is immediately hiring for a Clinical Trials Management Associate - III Position type: Full time Contract. Clinical Operations plays a key role in ensuring all client 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 client's products.
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Anticipates problems that may arise in clinical trials and develops solutions for these using precedents and original thinking. Description Senior Clinical Pharmacologist II:POSITION OVERVIEW: With considerable independence, you will typically lead clinical pharmacology studies of increasing complexity in Virology focusing on HIV therapeutics, which range from first-in human through approval and post-marketing activities including pediatric development.
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The Clinical Data Manager will be responsible for daily data management tasks for all phases of clinical trials including CRO/vendor oversight and support other functional areas such as clinical operations, statistical programming, and biostatistics.
$130,000 - $165,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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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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Bilingual Clinical Research Coordinator for Cognitive Aging Studies. The Stanford ADRC seeks a full-time bilingual Clinical Research Coordinator Associate. Under the supervision of ADRC principal investigator (Dr. Victor Henderson) and clinical coordinator, main duties include in-person and telephone recruitment of research participants; obtaining informed consent; scheduling and coordination of research participant visits; maintaining longitudinal contact with participants by phone, email and other means; data collection (particularly including psychometric data), scoring, and entry.
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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 Gilead’s products.
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In collaboration with a therapeutic area, the Scientific Director, Clinical Science will lead the design, conduct, analysis, and reporting of clinical trials. Knowledge of clinical trial methodology, regulatory and compliance requirements governing clinical trials and experience in the design of study protocols.
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Clinical Operations plays a key role in ensuring all 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 products.
$86 - $90 an hourExpandApply NowActive JobUpdated 15 days ago - UpvoteDownvoteShare Job
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Identifies and facilitates execution on growth opportunities with Diabetes Sales and Clinical Support Team. Medtronic is seeking a Clinical Territory Manager (CTM) to support the education and training of the company's products to Health Care Professionals and patients.
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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.
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Clinical Operations is responsible for the worldwide execution of all Phase I - IV clinical trials across all clients therapeutic areas. Clinical Trials Management Associate - III.
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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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Experience in clinical trial supplies required; supply chain/distribution logistics/import export/customs experience a plus. The core responsibilities include on-time delivery of study drug to patients/subjects and management of the clinical supply chain (packaging, labeling, distribution, inventory management, returns, and destruction of IMP/CTM.
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Maintaining clinic census goals
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Title: clinical trials Company: Hennepin Healthcare Research Institute in Foster City, CA
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