Pharmaceutical Regulatory Affairs Jobs in Marlborough

Assoc Director, US Ad/Promo Regulatory Review, GI (USBU) Review serves ... biologic products. Capable of providing regulatory strategic oversight for at least ... area/multiple products to help ensure regulatory compliance..

Manager, US Medical Ad/Promo Regulatory Duties: Works collaboratively with colleagues ... Works collaboratively with colleagues in Regulatory Affairs, Medical, Legal, Commercial, and Compliance ... and Compliance organizations and applies Regulatory..

... clinical studies in accordance with regulatory requirements, Good ClinicalPractice (GCP) guidelines ... of essential studydocuments, such as regulatory and ethics committee documents for ... Liaison) at LMA (Local Medical..

Corporate Counsel, Antitrust The candidate will support the successful execution of the Company’s M&A strategy and timely completion of its M&A transactions: assess, advise on and manage antitrust risk; collaborate with ..

Team Lead, Regulatory Affairs CMC, Plasma-Derived Therapies Responsibilities: Proactively ... and implementation of innovative CMC regulatory strategies in close collaboration with ... and emerging markets. Maintains optimal Regulatory Affairs CMC..

... other brand attorneys, IP, Compliance, Regulatory and other business groups to ... brand attorney to commercial, medical affairs, market access, distribution and development ... teams including clinical, product development,..

... team supports FMC RTG Medical Affairs strategies as it relates to ... Compliance Program, including following all regulatory and division/company policy requirements.PRINCIPAL DUTIES ... contribute and support RTG Medical..

... of assigned program including Medical Affairs Company Sponsored Studies (MACS), Investigator ... external regional and country specific regulatory guidelines. May serve as the ... and document repositories per Medical..

Regulatory Affairs CMC Manager, Plasma-Derived Therapies Business ... and implementation of innovative CMC regulatory strategies in close collaboration with ... markets. Maintains optimal GRA CMC Regulatory Affairs effectiveness for ongoing..

Senior Corporate Counsel, US Market Access The candidate will serve as legal business partner to the US Specialty Market Access Business Unit Team, participating in regular extended leadership meetings and providing ..

GE’s Pharmaceutical Diagnostics (PDx), is searching for ... related to commercial contracting, medical affairs, R&D, regulatory compliance, strategic partnerships and Intellectual ... marketing, promotion, and commercialization of pharmaceutical products as..

Regulatory Affairs CMC Manager, Plasma-Derived Therapies Business ... and implementation of innovative CMC regulatory strategies in close collaboration with ... markets. Maintains optimal GRA CMC Regulatory Affairs effectiveness for ongoing..

Why Join Intellia? Our mission is to develop curative genome editing treatments that can positively transform the lives of people living with severe and life-threatening diseases. Beyond our science, we live ..

Director, Regulatory Affairs (Data Products) Responsibilities: Ensure that ... of a drug or diagnostic regulatory approval submission (e.g. NDA, PMA). ... PMA). Serve as the internal regulatory expert on software..

Why Join Intellia? Our mission is to develop curative genome editing treatments that can positively transform the lives of people living with severe and life-threatening diseases. Beyond our science, we live ..

Manager, Medical Ad/Promo Regulatory The candidate will serves as ... multiple brands; supports other Ad/Promo Regulatory team members. Independently provides regulatory guidance and expertise to promotional ... products(s) of responsibility..

... always steady. Jill E. Medical Affairs It’s very comforting to know ... 8 -10 years required, in pharmaceutical marketing, digital/omnichannel marketing, or related ... related commercial function within the..

Associate Director, US Medical Ad/Promo Regulatory Review The candidate will understand ... and interpret complex issues about regulatory requirements and promotional strategy. Mentor ... train and provide technical and regulatory..

... wholly owned subsidiary of Otsuka Pharmaceutical Co., Ltd. of Japan. Visterra ... to support nonclinical reports and regulatory submissions.rnrnThe Operations Specialist, Nonclinical Development ... will also work closely with..

Director, Regulatory Counsel Responsibilities: Provide legal support for the Sales, Marketing, Commercial Operations, Medical Affairs and Patient Advocacy functions, in the furtherance of their operational responsibilities and consistent with the requirements ..

... is a subsidiary of Otsuka Pharmaceutical Co., Ltd. of Japan. As ... mastery of the fundamentals of regulatory affairs, the Associate Director will have ... the Executive Director, Head..

Assistant General Counsel - R&D The candidate will be doing provision of general legal advice as needed to the Global R&D organization. Proactive monitoring and information to stakeholders of relevant changes ..

... reports for all GE Healthcare Pharmaceutical Diagnostics (PDx) products Support preparation ... regulations/guidance that impact post approval regulatory affairs Complete assigned training and maintain ... knowledge and understanding of..