Latest Drug Regulatory Affairs jobs in South Bound Brook, NJ

18 Drug Regulatory Affairs Jobs in South Bound Brook, NJ

Consumer Safety Officer Food and Drug Administration - South Bound Brook, New Jersey Services (DHHS), Food and Drug Administration (FDA), Office of Regulatory Affairs (ORA), Office of Medical Products and Tobacco Operations (OMPTO), Office of Biological Products Operations (OBPO), which 11 days ago
Senior Regulatory Affairs Associate Breckenridge Pharmaceutical, Inc. - Berkeley Heights, NJ, United States regulatory affairs operations. Knowledge of eCTD publishing systems and standards, EDMS technology and related publishing tools. Working knowledge of US FDA (OGD/CDER) e-submission requirements. Strong written 7 days ago
Associate Director, US Regulatory Affairs, Advertising & Promotion Proclinical Staffing - Morristown, 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 8 days ago
Associate Director, Clinical Sciences - Ophthalmology Johnson and Johnson - Raritan, NJ for clinical data review, including medical data review, coding, in conjunction with other clinical team members. OTHER RESPONSIBILITIES / DETAILED DUTIES: * Assists Regulatory Affairs in the development of drug 8 days ago
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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 28 days ago
Safety Case Management Product 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 23 days ago
Senior Director, Drug Development, Project Management - Rare Diseases (Pompe Disease) Shionogi Inc. - Florham Park, New Jersey throughout the project lifecycle. Collaborate with cross-functional teams including research, clinical development, medical and regulatory affairs, and commercial teams to drive successful drug development 2 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 25 days ago
Chief Medical Officer - Gene Therapy and Rare Disease i-Pharm Consulting - Trenton, NJ, United States and build out the full R&D organization including clinical development, clinical operations, regulatory affairs, biometrics, medical affairs and drug safety Oversee design and execution of global clinical 13 days ago
Senior Director, Global Regulatory Leader, CAR-T Therapy Johnson & Johnson - Raritan, NJ affairs experience A track record of innovative scientific thinking and application is required Significant experience in the development and execution of global regulatory strategies, the drug development USD 187,000.00 - 322,000.00 per year 22 days ago

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