Latest Drug Regulatory Affairs jobs in Summit, NJ

21 Drug Regulatory Affairs Jobs in Summit, NJ

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
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 17 days ago
Senior Trial Manager, Clinical Operations Shionogi Inc. - Florham Park, New Jersey including Pharmacovigilance, Drug Supply, Quality Assurance, Regulatory Affairs, Legal, Medical Writing, Biostatistics and Data Management to meet program objectives and support achievement of goals 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. 14 days ago
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Senior Director, Drug Development, Project Management - Rare Diseases Shionogi Inc. - Florham Park, New Jersey financial accountability throughout the project lifecycle. Collaborate with cross-functional teams including research, clinical development, medical and regulatory affairs, and commercial teams to drive 2 days ago
Principal Scientist, Clinical Research, Thoracic Malignancies Merck - Rahway, NJ 07065 Scientists in the execution of clinical studies; Work closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development 10 days ago
Senior Principal Scientist, Clinical Research, Hematology/Lymphoma Merck - Rahway, NJ 07065 , the Senior Director may: Supervise the activities of Clinical Scientists in the execution of clinical studies Work closely with a cross-functional group of experts in commercialization, regulatory affairs 23 days ago
Consumer Safety Officer Food and Drug Administration - Union, Washington (FDA), Office of Regulatory Affairs (ORA), Office of Medical Product and Tobacco Operations (OMPTO), Office of Medical Device and Radiological Health Operations (OMDRHO). The incumbent provides advice 11 days ago
Senior Principal Scientist, Thoracic Malignancies Merck - Rahway, NJ 07065 , the The Senior Director may: Supervise the activities of Clinical Scientists in the execution of clinical studies Work closely with a cross-functional group of experts in commercialization, regulatory affairs 10 days ago
Principal Scientist, Hematology-Oncology Merck - Rahway, NJ 07065 the activities of Clinical Scientists in the execution of clinical studies. Work closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage 23 days ago

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