- Merck & Co. (Rahway, NJ)
- …learn new processes and technologies. Broad knowledge of Clinical Development and Regulatory Affairs requirements. The ability to multi-task, work independently, ... and coordinating CDS technical initiatives. Supporting the clinical database manager /supervisor in project planning, manpower projections, and resource allocation… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …market access, commercial effectiveness, sales, medical/CMR, legal, compliance, and regulatory . Other internal relationships include Public Affairs , Government ... short- and long-term business plans, results and follow up Must have solid understanding of the pharmaceutical marketplace including legal, medical, regulatory … more
- Teva Pharmaceuticals (Parsippany, NJ)
- Manager Regulatory Affairs Date: Sep 9, 2024 Location: Parsippany, United States, New Jersey, 07054 Company: Teva Pharmaceuticals Job Id: 57668 **Who we ... **The opportunity** Teva Pharmaceuticals USA, Inc. is seeking a Regulatory Affairs Manager (Parsippany, NJ)...(ANDA's) and associated amendments, for various dosage forms (solutions, solid oral, semi- solid , or combination products). +… more
- L'Oreal USA (Clark, NJ)
- …/ Job Search (https://careers.loreal.com/en\_US/jobs/SearchJobs) / 187151 Scientist, Regulatory Affairs , L'Oreal Research & Innovation ... & Innovation Full - Time 22-Aug-2024 Position Title: Scientist, Regulatory Affairs , L'Oreal Research & Innovation Location...time management skills. + Strong problem solving skills + Solid oral and written communication skills is required +… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- …have:** + Minimum Bachelor's Degree. Advanced life science degree or certification in Regulatory Affairs Sciences preferred. + Minimum of 5 years' experience in ... Regeneron is seeking a Manager to join the Regulatory Intelligence...the biotech/pharmaceutical industry or health authority + Solid understanding of the drug development and commercialization process,… more
- Mitsubishi Chemical Group (Jersey City, NJ)
- …medical analyses for risk characterization to develop Risk Management Plans (RMPs). The Manager will also draft responses for regulatory authority inquires on ... at least 2 years of experience in US and international Drug Safety. + Solid understanding of scientific principles and regulatory requirements relevant to global… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- …you if can:** + Interact with Medical Directors, Clinical Scientists, Regulatory Affairs , Preclinical scientists, Statistical Programming, Data Management, ... and processes, and influence the external pharmaceutical industry and regulatory environment through participation in professional associations, conferences, and… more
- KPMG (New York, NY)
- **Business Title:** Manager , Transfer Pricing **Requisition Number:** 111969 - 68 **Function:** Tax Services **Area of Interest:** **State:** NY **City:** New York ... for as a firm KPMG is currently seeking a Manager to join our Transfer Pricing (https://tax.kpmg.us/services/transfer-pricing.html) practice. Responsibilities: +… more
- The Mount Sinai Health System (New York, NY)
- …Review Board), IACUC (Institutional Animal Care Use Committee), Research Compliance, Regulatory Affairs and Grants + Oversee implementation of Research ... **JOB DESCRIPTION** **IT Project Manager II - Scholarly and Research Technologies -...preferred) or healthcare and technology related fields. + Requires solid project management skills, ability to multitask and manage… more
- TD Bank (New York, NY)
- …working relationships between all areas of Risk Management, including Regulators, Government Affairs , Legal, and Compliance. Ensures regulatory and risk issues ... regarding the treasury functions and capital management and have solid experience in risk management, we would love to...understood, analyzed, and measured as part of the Bank's regulatory and local frameworks. You are required to demonstrate… more
- Merck (Rahway, NJ)
- …new processes and technologies. + Broad knowledge of Clinical Development and Regulatory Affairs requirements. + The ability to multi-task, work independently, ... coordinating CDS technical initiatives. + Supporting the clinical database manager /supervisor in project planning, manpower projections, and resource allocation… more
