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Found 69 jobs
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Sr. Human Subjects Protection Specialist
The Sr HSPS will execute the following support services: Provide comprehensive, timely, professional quality and fully documented reviews of resea...
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Scientist I - Hemorrhage & Resuscitation (Large animals)
General Dynamics IT is seeking a Scientist I to support the following research project at the Naval Medical Research Unit in San Antonio, Texas. Pr...
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Scientist IV Microbiology
The Principle Investigator will conduct research on specified bacterial threats; in support of the biodefense and infectious disease program. The P...
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CDMRP Science Officer - Fort Detrick
The USAMRMC is a major subordinate Command of the United States Army Medical Command. The Commanding General, USAMRMC, directs the management of a ...
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Social Scientist
Westat is an employee-owned corporation providing research services to agencies of the U.S. Government, as well as businesses, foundations, and sta...
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Senior Environmental Scientist
Dewberry is a leading, market-facing professional services firm with more than 50 locations and 2,000 professionals nationwide. What sets us apart ...
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Business Analyst-Clinical Systems Analyst
Manage a project’s software development life cycle for data capture applications (i.e., AdvantageEDC, GlobalTrace, etc.) from requirements gathering
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Talent Director
Work in collaboration with Emmes Project Leaders and Functional Group Managers to manage the internal deployment of talent in accordance with contrac
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IRB Local Context Coordinator
Responsible for reviewing and processing all submissions from participating institutions for completeness before CIRB review and complete an administ
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Administrative Coordinator
Provide day-to-day coordination between operational staff Aid in the design, development consolidation and distribution of reports, manuals, presenta
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Data Manager/Protocol Monitor
Strong data management/computer skills; experience with CRF design, EDC systems, or other web based data collection systems helpful Attention to deta
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Data Manager/Protocol Monitor
Strong data management/computer skills; experience with CRF design, EDC systems, or other web based data collection systems helpful Attention to deta
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Regulatory Affairs Specialist
Participates in the development of regulatory strategies to advance new drugs, biologics, and devices through the clinical trial and licensure proces
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IRB Local Context Coordinator
Responsible for reviewing and processing all submissions from participating institutions for completeness before CIRB review and complete an administ
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Clinical Protocol Specialist
Possesses detailed knowledge of the protocol and its associated activities and timelines Participates in the preparation and/or review of protocol an
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Clinical Protocol Specialist
Possesses detailed knowledge of the protocol and its associated activities and timelines Participates in the preparation and/or review of protocol an
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Clinical Data Manager
Work in a team environment to design, develop and manage clinical trial data systems, supporting materials, and processes, including the EMMES propri
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CDISC Data Manager
Review protocols for CDISC conformance Develop and review Case Report Forms and eCRFs with CDISC CDASH and SDTM conformant elements Utilize proprieta
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CDISC Data Manager
Review protocols for CDISC conformance Develop and review Case Report Forms and eCRFs with CDISC CDASH and SDTM conformant elements Utilize proprieta
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CRA Manager
Coordinates all monitoring aspects in the execution and support of clinical trial activities Supervises and ensures CRA team members are compliant wi
