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Exceptional knowledge of EC/IRB regulations, regulatory document requirements, expectations, and monitoring of the Trial Master File (TMF). Exceptional knowledge of EC/IRB regulations, regulatory document requirements, expectations, and monitoring of the Trial Master File (TMF.
$138,500 - $153,100 a yearFull-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Act as a resource for the research studies' regulatory activities including, but not limited to, interpreting, preparation, coordination, implementation and compliance with the Institutional Review Board (IRB) guidelines, FDA requirements, and Good Clinical Practice procedures.
$82,500 - $120,000 a yearExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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In addition to the utilization of portable, rapid assay technologies to identify pathogens in the field, test specimens and limited epidemiologic data, when approved by the Institutional Review Board (IRB), are provided to the NHRC laboratory where diagnostics and, in some instances, in-depth pathogen characterization is conducted.
ExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Participate in the development of clinical trial protocols, amendments, CRFs, IRB/Ethics applications, and recruitment materials. Manage and oversee the operational aspects of Insmed's clinical trials, including vendors such as central labs, biomarker and specialty laboratories, clinical trial sites, etc.
Full-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Any qualifications to be considered as equivalents, in lieu of stated minimums, require the prior approval of the Chief Human Resources Officer. This position will be in support of Naval Health Research Center (NHRC), Operational Infectious Diseases (OID.
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Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB). Works within the core to establish efficient and comprehensive procedures for compliance with CSMC IRB and external sponsors for the conduct of routine and regular clinical research, IIT monitoring and audits.
Part-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Experience creating Informed Consent Documents that comply with HRPP/UCSD IRB policies and procedures, FDA regulations, and sponsor requirements. Working knowledge of UCSD Human Research Protections Program (HRPP/IRB) policies and Procedures.
ExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Additional tasks consist of assisting with Data Licensing Agreements (DLAs) with Law, Institutional Review Board (IRB) process, attend HHS Business Users of Data (HHS BUD) meeting with Director of Performance Management, ensure travel arrangements for conferences are done for the team, attend P3 management meetings, all staff and other meetings.
ExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Execute assigned clinical trials including start up, subject recruitment & scheduling, consenting, screening, subject training, collection of regulatory documents, conducting study visits, performing SMBG testing, ensuring data is entered in a timely manner and all queries are resolved, managing, and reporting adverse events, serious adverse events, and deviations, and providing IRB close-out reports.
$35 - $45 an hourFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Prepare, organize, and submit required research documentation in order to obtain research approvals, such as military approval, protection of human subjects IRB approval. All Native Group is seeking an Epidemiologist to provide travel support for the Defense Health Agency DoD HIV/AIDS Prevention Program Project Management Support Services program.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Screen and consent participants, prepare and submit regulatory documents and reports to IRB and funding sites, oversee all aspects of study flow. Under supervision of the lab manager and lead investigator, performs clinical research work for clinical trials focused on treating posttraumatic stress disorder (PTSD) and related problems (e.
ExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Manages clinical sites and academics institutions, ensures adherence for keeping clinical records, source documents, data entry, manages clinical trial logistics, applications (IRB, local agencies.
$150,000 - $165,000 a yearFull-timeExpandUpdated 2 months ago - UpvoteDownvoteShare Job
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You will have oversight of the development and administration of research ethics training to scientists and support staff as well as to members of the Institutional Review Board (IRB). You will have oversight of the development and administration of research ethics training to scientists and support staff as well as to members of the Institutional Review Board (IRB.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Experience in rare disease and/or orphan indications is preferred. Provide leadership and management of a clinical study(s) and clinical operations aspects of one or more drug development program(s) in compliance with GCP and relevant regulatory guidelines.
$175,000 - $241,667 a yearFull-timeExpandApply NowActive JobUpdated 25 days ago - UpvoteDownvoteShare Job
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Assist with supporting efforts across the full research project cycle, including, but not limited to: reviewing relevant literature; project conceptualization; proposal development and submission; project documentation and compliance (e.g., IRB protocol, data-sharing agreements, survey approval, etc.
Part-timeExpandApply NowActive JobUpdated 14 days ago
irb job in San Diego, CA
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