Latest Drug Regulatory Affairs jobs in New Jersey

25 Drug Regulatory Affairs Jobs in New Jersey

Onsite // Oncology Associate Director Global Regulatory Lead Talent Groups - Jersey City, NJ, United States environment with colleagues throughout GRS Education Requirements: Ph.D., M.D., PharmD., MS or commensurate experience Experience Requirements: Significant experience in regulatory affairs (e.g., 3-5 years) Key Yesterday
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 22 days ago
Principal Scientist, Clinical Research, Breast Cancer Merck - Rahway, NJ 07065 closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects; and Assist the Senior/Executive Director 8 days ago
Associate Director, US Regulatory Affairs, Advertising & Promotion Proclinical Staffing - Plainsboro, NJ, United States Regulatory Affairs representative, you will work with brand on competitively positioning assigned products appropriately while maintaining compliance with applicable FDA regulations, company policies 5 days ago
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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 22 days ago
Senior Director, Global Regulatory Leader, CAR-T Therapy Johnson and Johnson - Raritan, NJ years in drug development any of the following areas (e.g. Global Regulatory Affairs, R&D or health authority role) is required. * 10 years within the pharmaceutical/biotech industry is required, along 2 days ago
Director, Regulatory Affairs Strategy NS Pharma, Inc. - Paramus, NJ, United States and other health authority guidances/guidelines. Experience in rare disease/accelerated approvals preferred. Regulatory Affairs Certification is a plus. 22 days ago
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 22 days ago
Director, Global Regulatory Leader (GRL) (1 of 2) Johnson and Johnson - Titusville, NJ : * A minimum of 8 years' experience in either pharmaceutical industry, medical device industry, consumer industry or health authority regulated industry * At least 6 years of Regulatory Affairs experience 3 days ago
Senior Regulatory Affairs Associate Breckenridge Pharmaceutical, Inc. - Berkeley Heights, NJ, United States and through strategic partnerships with manufactures from around the world. JOB SUMMARY: The Senior Associate, Regulatory Affairs is responsible for supporting applications under pre and post approval 25 days ago

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