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The Clinical Research Coordinator will perform independently to execute, manage, and coordinate research protocols, as directed by the Clinical Research Manager and/or the Principal Investigator (PI), and/or the Associate Director for the Clinical Research Programs.
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It has direct responsibility for implementing a diverse portfolio of research activities for one or more studies which may include multicenter clinical trials (both NIH and industry-sponsored), local investigator-initiated clinical trials, and/or programmatic clinical research activities, such as a clinical database and biorepository.
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Drive planning for key drug development stage-gate decision points (FIH, regulatory filings, study start-up, etc.) In addition to TVE, our technology includes a robust AAV manufacturing platform and onsite manufacturing facility that allows us to rapidly produce and test research grade material and scale up to GMP clinical material.
$265,000 - $314,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Completion of UCSF Clinical Research Study Coordinator training. The Division of Neuro-Oncology Clinical Trials Program is an active research program that includes studies supported by pharmaceutical industry; investigator-initiated studies in collaboration with outside universities; NCI-cooperative groups.
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As lead of the Study Core Team the CS will lead via a matrix organization Epidemiology, Biostats, Clinical Operations, Medical/Scientific Affairs, Regional, Pfizer laboratory assay group, and external team members.
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8+ years of clinical study management experience in registries, observational research, RWD/E, or clinical trials as a clinical study lead/project manager. Verily’s Clinical Studies Platform (CSP) business is focused on transforming evidence generation within clinical research.
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This role is responsible for overseeing all aspects of drug safety study operational activities from study start up to close out. Oversee Drug Safety Study Team Leads activities including review of study protocols, case report forms, Investigator Brochures and participation on IND Annual Reports in support of the Drug Safety Physician.
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Review development of site and CRA training materials and presentation at SIV and Investigator meetings and support on Study committee (e.g., DMC) activities. + Proficient knowledge of GCP/ICH, drug development process, study design, statistics, clinical operations.
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Reporting to the Head of Clinical Development, this individual will have oversight of and accountability for clinical trials from study start-up to BLA approval. Contribute to the design, start-up, execution, analysis and communication of the clinical studies for a product candidate.
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Following the Ph. D., 2+ years of mathematical modeling & computer simulation experience in the pharmaceutical industry for the Sr. Research Investigator level or 5+ years for the Associate Director level.
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The primary focus of this role is to provide legal contracting support with the guidance of Contracts Counsel for Sana’s research, manufacturing, and clinical activities as well as general business, operational and organization-wide contracting support.
$130,000 - $165,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Applicants for all Criminal Investigator (Special Agent) 1811 positions must meet all GS-1811 Criminal Investigator (Special Agent) Qualification Standards, including Medical Requirements, please see.
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Under the direct supervision of the Senior Study Coordinator, Investigator-Initiated Studies (IDS), the Program Assistant will be part of a dynamic team conducting HIV preventive vaccine studies, HIV pre-exposure prophylaxis (PrEP) studies, including oral and injectable medications, and other studies of biomedical STI and HIV prevention strategies.
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Environmental/public health research at multiple levels and is comfortable with study design, research, whenever possible, encourage group leaders to communicate study results to their.
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The Clinical Research Coordinator (CRC) is a specialized research professional working with and under the direction of the clinical Principal Investigator (PI), Manager of Compliance and Contracts, and the Administrative Nurse II.
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clinical research investigator study start up jobs Company: Cedars Sinai in San Francisco, CA
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