Latest Drug Regulatory Affairs jobs in Paramus, NJ

15 Drug Regulatory Affairs Jobs in Paramus, NJ

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
Clinical Supplies Manager SK Life Science, Inc. - Paramus, New Jersey experiences, etc. Manage and processing of CMC Team project invoices and internal project budget requests (ARIBA), and monitoring of project financial tracking. Assist and support Regulatory Affairs (RA 13 days ago
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
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
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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
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
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 10 days ago
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 10 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 18 days ago
Program Manager, Clinical Database Services Merck - Rahway, NJ 07065 Team. Strong organizational, time management, and multi-project coordination skills Broad knowledge of Clinical Development and Regulatory Affairs requirements Ability to multi-task, work independently 7 days ago

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