Latest Medical Affairs Drug Safety jobs - JobisJob United States Mobile

18 Medical Affairs Drug Safety Jobs

Medical Officer (TB Clinical Research) - NIH Kelly - Rockville, MD, United States particularly the safety of the drug in question (5) Evaluate annual IND annual reports for medical safety and report findings to Regulatory Affairs Branch (RAB). (6) Provide medical expertise in protocol follow 5 days ago
QSP Modeling Head (AD / Dir / SD level) | Global Pharma – Oncology & CNS | New York Metro Area (hybrid) | RETAINED SEARCH Cornerstone Search Group - , NJ, United States Development / Medical Affairs / Drug Safety: 75+ retained assignments HEOR/RWE/Market Access (AD/Director/SD/ED levels): 100+ retained assignments Cornerstone’s Privacy Policy: Cornerstone Search Group 13 days ago
Medical Information & Scientific Communications Manager CSL Vifor - Coffeyville, Kansas platforms, IRMS, Microsoft, and Adobe applications Experience with review of medical or promotional content. Experience with regulatory, drug safety, and legal implications of Medical Affairs activities, e.g 2 days ago
Regulatory Affairs Specialist Planet Pharma - , NC, United States (in cooperation with Medical Affairs). Responsible for review of investigational product release-enabling documents. Primary or secondary responsibility for training company employees in regulatory practices 12 days ago
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GPV Submission Specialist GForce Life Sciences - Princeton, NJ, United States preferred to be in Bachelor of Science or related healthcare degree 1-3 years of Submission Experience Demonstrated proficiency in safety database functionality *Drug Safety experience is defined as actual 14 days ago
Director, Safety Physician - Remote Emergent Biosolutions - Gaithersburg, MD, US reports including medical analysis. • Thorough understanding of the cross functional drug development processes (Clinical Operations, Biometrics, and Regulatory Affairs) and context applicable to safety 4 days ago
GPV Case Management Product Specialist GForce Life Sciences - Trenton, NJ, United States preferred to be in Bachelor of Science or related healthcare degree 1-3 years of Submission Experience Demonstrated proficiency in safety database functionality *Drug Safety experience is defined as actual 14 days ago
Senior Pharmacovigilance Associate Tandym Group - Florham Park, NJ, United States per device safety reporting requirements In-depth knowledge of the Drug Development process, Signal Detection, and Regulatory Affairs In-depth knowledge of Domestic and Global Safety regulations Profound 14 days ago
Director, Medical Safety Officer: Immunology Johnson and Johnson - Titusville, NJ and Experience: • Physician (MD or equivalent) with a minimum of 2 years of pharmacovigilance experience or other relevant experience (e.g. Clinical research, Medical Affairs) • Demonstrated skills in clinical 2 days ago
Associate Director Regulatory Affairs, Labeling BioPhase - , CA, United States with internal stakeholders including Regulatory Affairs, Clinical Research, Drug Safety, Quality, Commercial, Medical Affairs, Legal, Manufacturing, and Supply Chain. Lead cross-functional labeling forums 23 days ago

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