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Regulatory Affairs Jobs in Frederick (MD)

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Search Results - Regulatory Affairs Jobs in Frederick (MD)
Allied Technologies and Consulting, LLC.-Frederick (MD)
JOB DESCRIPTION: Allied Technologies and Consulting (ATC) is recruiting for a Regulatory Affairs Subject Matter Expert (SME) to provide senior-level regulatory leadership, technical expertise, and strategic guidance in support of medical product...
Allied Technologies & Consulting-Frederick (MD)
Job Description Job Description JOB DESCRIPTION: Allied Technologies and Consulting (ATC) is recruiting for a Regulatory Affairs Subject Matter Expert (SME) to provide senior-level regulatory leadership, technical expertise, and strategic...
Keaki Technologies-Frederick (MD)
Bering-Alaka`ina Holdings, LLC is looking for has a potential need for a Regulatory Affairs Support Subject Matter Expert to provide support for our government customer in Frederick, MD at Fort Detrick Army Base. DESCRIPTION OF RESPONSIBILITIES...
Frederick (MD)
Position Summary: Odyssey is looking for a Regulatory Affairs Support (Warfighter Expeditionary Medicine and Treatment) to support the Defense Health Agency (DHA) located at Ft. Detrick, MD. This Regulatory Affairs Support SME provides...
icims.com -
Systems Plus, Inc.-Frederick (MD)
to identify regulatory affairs strategies to optimize product development across the portfolio.  •  Review and analyze summaries, progress reports, clinical protocols, investigator brochures, and safety profiles and safety surveillance data.  •  Facilitate...
Systems Plus, Inc.-Frederick (MD)
Daily Responsibilities: Help bring breakthrough medical technologies to the Warfighter by supporting the regulatory pathways that move innovative products from development to deployment. In this role, you will work closely with scientists...
Systems Plus, Inc.-Frederick (MD)
JTS) to develop Clinical Practice Guideline(s) in support of the full rate decision or off-label use of the materiel solution.  •  Collaborate to identify regulatory affairs (RA) strategies will optimize product development.  •  Review and analyze summaries...
Keaki Technologies-Frederick (MD)
of development. * Coordinate and assist with Joint Trauma System (JTS) to develop Clinical Practice Guideline(s) in support of the full rate decision or off-label use of the materiel solution. * Collaborate as necessary to identify regulatory affairs (RA)...
Keaki Technologies-Frederick (MD)
of development. * Coordinate and assist with Joint Trauma System (JTS) to develop Clinical Practice Guideline(s) in support of the full rate decision or off-label use of the materiel solution. * Collaborate as necessary to identify regulatory affairs (RA)...
Keaki Technologies-Frederick (MD)
as necessary to identify regulatory affairs (RA) strategies that will optimize product development. * Review and analyze summaries, progress reports, clinical protocols, investigator brochures, and safety profiles and safety surveillance data. * Facilitate...

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