- Merck & Co. (Rahway, NJ)
- …and Scientific Affairs (GMSA) (referred to as EDMA) is accountable for the development and execution of scientific & medical affairs plans for their assigned ... skills Preferred Experience and Skills: At least 5 years global or US medical affairs or clinical development experience with proven track record of contribution… more
- Merck & Co. (Upper Gwynedd, PA)
- … Regulatory Compliance, Microbiology, Molecular Microbiology, Pharmaceutical Process Development , Regulatory Affairs Compliance, Regulatory Affairs ... the preparation and submission of CMC dossiers for all assigned development products. -Primary responsibilities include, but are not limited to:Regulatory… more
- Eisai, Inc (Nutley, NJ)
- …through in neurology and oncology, with a strong emphasis on research and development . Our history includes the development of many innovative medicines, notably ... profile, we want to hear from you. The Associate Director (AD), Global Medical Affairs Training and Education is responsible for the planning and execution of Global… more
- Merck & Co. (North Wales, PA)
- …and prioritization skills.PreferredAdvanced degree (MD, PharmD, PhD).Experience with the development of Global or Regional Medical/Scientific Affairs ... Implementation (V&I) organization, which includes Global Medical and Scientific Affairs as well as Outcomes Research.This mid-level, headquarters-based position… more
- Eisai, Inc (Nutley, NJ)
- …through in neurology and oncology, with a strong emphasis on research and development . Our history includes the development of many innovative medicines, notably ... of relevant medical communications deliverables aligned with the Medical Affairs strategic plan for assigned therapeutic area(s). These deliverables include… more
- Genmab (NJ)
- …of an exciting opportunity of a passionate, high profile, high-impact Global Medical Affairs team, and work in a dynamic and collaborative setting.The MSL/Sr. MSL is ... specialists who function as an extension of the Global Medical Affairs organization. MSLs are responsible for developing and enhancing professional relationships… more
- Merck & Co. (North Wales, PA)
- …reimbursement. The incumbent is expected to work cross-functionally with clinical development , medical affairs , biostatistics, market access, commercial, and ... resides in the V&I organization, which includes Global Medical and Scientific Affairs as well as Outcomes Research, and will support Pneumococcal Vaccines.Under the… more
- Eisai, Inc (Nutley, NJ)
- …information between Key Opinion Leaders (KOLs)/investigators and the company's Medical Affairs and development groups.Establish, foster, cultivate and maintain ... and oncology, with a strong emphasis on research and development . Our history includes the development of...(Sr. MSL) is a field-facing representative of US Medical Affairs with a primary responsibility of engaging in the… more
- Merck & Co. (Rahway, NJ)
- …submissions. The incumbent is expected to work cross-functionally with clinical development , medical affairs , biostatistics, market access, commercial and ... reviews and meta-analyses, and economic modelling. Key responsibilities also include development of American Managed Care Pharmacy (AMCP) dossiers for US payers,… more
- Genmab (NJ)
- …and Intelligence Associate Director will primarily be responsible for leading the development and maintenance of global labeling documents (eg, Core Data Sheet, ... policy and/or intelligence deliverables. This role will be within Global Regulatory Affairs (GRA) and will report to the Sr. Director, Labeling, Policy and… more
- Merck & Co. (North Wales, PA)
- …reimbursement. The incumbent is expected to work cross-functionally with clinical development , medical affairs , biostatistics, market access, commercial and ... reviews and meta-analyses, and economic modelling. Key responsibilities also include development of American Managed Care Pharmacy (AMCP) dossiers for US payers,… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Process Manager will be a key member of the Global Regulatory Affairs (GRA) Process Excellence & Analytics function, responsible for ensuring Daiichi Sankyo's ... compliant with relevant regulations. This role will work with Global Regulatory Affairs and cross-functional teams (eg, Quality, CSPV, Clinical Operations, Clinical … more
- Eisai, Inc (San Francisco, CA)
- …through in neurology and oncology, with a strong emphasis on research and development . Our history includes the development of many innovative medicines, notably ... or Principal Medical Science Liaison) is a field-facing representative of US Medical Affairs with a primary responsibility of engaging in the exchange of scientific… more
- Katalyst HealthCares and Life Sciences (Boston, MA)
- Responsibilities: The role requires strong US, EU, China, and international regulatory experience that can be leveraged to help support international expansion. ... Provides technical guidance and regulatory training/mentoring to other Regulatory Affairs employees and cross-functional teams. Acts as company representative,… more
- Housing Authority of the City of Los Angeles, CA (Los Angeles, CA)
- …Angeles, CA Job Type: At-Will Exempt Job Number: 25-44 Department: Community Affairs Opening Date: 06/23/2025 Characteristics of the Class: Under general direction ... from the Chief of Community Affairs , the Deputy Director of Community Affairs ...Work Source Center, management of HUD-required Resident Advisory Councils, development of unique tools for community engagement and growth… more
- Capstan (Santa Cruz, CA)
- Reports to: Head of Regulatory Affairs (SVP, RA) Workplace type: Hybrid Description: This is a unique opportunity for an experienced Regulatory Affairs ... start-up positioned to revolutionize structural heart care. The Manager of Regulatory Affairs will help build and execute the regulatory strategy for our novel… more
- Cleerly (Denver, CO)
- …cardiologists and are a growing team of world-class engineering, operations, medical affairs , marketing, and sales leaders. We raised $223M in Series C funding ... in the job description. About the Opportunity As Principal Regulatory Affairs Specialist, you will provide regulatory support and strategy development… more
- Elliquence (Baldwin, NY)
- We are seeking an experienced Product Development Manager with a strong background in engineering and project management to lead the development and innovation ... ideal candidate will have significant expertise in medical device development , regulatory compliance, cross-functional project management, and supplier … more
- Vertex Pharmaceuticals (Boston, MA)
- Job Description General Summary: The Clinical Development Medical Director will serve as the Medical Lead for Vertex clinical trials, working with cross-functional ... work on multiple trials in all Phases of clinical development and may also participate in other selected projects... and other internal groups at Vertex (eg, Regulatory Affairs , Clinical Operations) for assigned studies Represents Vertex to… more
- Abbott (Sylmar, CA)
- …be your true self and live a full life. You'll also have access to: Career development with an international company where you can grow the career you dream of ... products. Coordinates with Engineering, Marketing, Clinical Research, and Regulatory Affairs to define product labeling requirements. Designs and updates… more
