- Merck & Co. (Rahway, NJ)
- …The individual functions with a high degree of independence and provides regulatory oversight for assigned products, to optimize product labeling and ... Job DescriptionWe are seeking a Director (Principal Scientist), Global Regulatory Affairs Liaison with a visionary, growth-oriented mindset that can help advance… more
- Merck & Co. (Rahway, NJ)
- …The individual functions with a high degree of independence and provides regulatory oversight for assigned products, to optimize product labeling and ... Job DescriptionWe are seeking a Senior Director (Sr. Principal Scientist) Global Regulatory Affairs Liaison with a visionary, growth-oriented mindset that can… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …immune disorders. Summary: This position (GRL Oncology) is responsible for providing oversight and formulation of strategy for global regulatory submissions in ... EU, Japan, China, and other regions. This position ensures alignment of regulatory strategies within the department and adherence to therapeutic area direction and… more
- Merck & Co. (Millsboro, DE)
- …Delaware seeks to add an Attending Veterinarian in the role of Associate Director .This position will have overall responsibility for oversight and administration ... Job DescriptionAssociate Director , Animal ServicesAbout the JobAnimal Health in Millsboro...care and use of animals.Responsibilities also include training and oversight of the animal care staff, serving as a… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …relevant duties under the RDPV QA function to ensure that Quality assurance oversight are being addressed and managed appropriately. Ability to exercise influence at ... Implementing strategic and tactical plans to drive sustainable improvements.Supports Regulatory Affairs in providing quality content and review of documents… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …rare diseases and immune disorders. SummaryThis position serves as the Global Regulatory Affairs (GRA) Labeling Strategy expert to the Global Product Team (GPT) ... operational leadership on new product labeling in collaboration with the Global Regulatory Leads (GRLs) and Clinical Safety & Pharmacovigilance (CSPV) for assigned… more
- Insmed Incorporated (San Diego, CA)
- …for Millennials™, and Best Medium Workplaces™ lists.OverviewThe Executive Medical Director of Ophthalmology, Clinical Development holds the responsibility to lead ... individual will be the primary point person for medical monitoring and oversight of assigned clinical programs including monitoring of clinical studies, review &… more
- Eisai, Inc (Nutley, NJ)
- …a difference. If this is your profile, we want to hear from you.The Director , Global IT Governance, Risk & Controls Management Lead is responsible for overseeing the ... strategic and execution perspectives for Eisai. Reporting directly to the Executive Director , IT Security, Compliance, & Architecture, s/he is the Global IT… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …areas centered around rare diseases and immune disorders.Summary The Senior Director sits within Global Oncology Clinical Development, an organization dedicated to ... Summary / Objective Serves as a primary source of medical accountability and oversight for one or more clinical trials Matrix management responsibilities across the… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …as we embark on shaping our future. The Position The Associate Director , HCP Experience has overall strategic and operational responsibility as well as ... and Engagement, Customer Experience and Marketing Enablement, Employee Experience, Regulatory , PRB, PSP, FRM, Conventions, Global Marketing, Launch Office,… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- Director , Clinical Development Join a Legacy of Innovation 125 Years and Counting!Daiichi Sankyo Group is dedicated to the creation and supply of innovative ... Job Summary: Serves as a primary source of medical accountability and oversight for one or more clinical trials Matrix management responsibilities across the… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …areas centered around rare diseases and immune disorders. SummaryThe Senior Director sits within Global Oncology Clinical Development, an organization dedicated to ... clinical trials. Serves as a primary source of medical accountability and oversight for one or more clinical trials Matrix management responsibilities across the… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Clinical Operations, Clinical Development, Biostatistics and Data Management, Regulatory Affairs, Quantitative Clinical Pharmacology, Clinical Safety and ... Pharmacovigilance, Regulatory /Risk Management, Quality Assurance, Medical Affairs, Translational Research, Research,...functions of Daiichi Sankyo. As a trusted partner, provide oversight of technical and solutions architecture and design for… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Clinical Operations, Clinical Development, Biostatistics and Data Management, Regulatory Affairs, Quantitative Clinical Pharmacology, Clinical Safety and ... Pharmacovigilance, Regulatory /Risk Management, Quality Assurance, Medical Affairs, Translational Research, Research,...functions of Daiichi Sankyo. As a trusted partner, provide oversight of business demand to balance R&D IT portfolio… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …and Senior Global Safety Scientists and Safety Scientists. Contributes and provides oversight in the development of safety strategy and safety deliverables for ... and external stakeholders. Relationships This position will report to Senior Director Safety Surveillance, US East Coast Development Hub. Key internal stakeholders… more
- Merck & Co. (San Diego, CA)
- …that can be deployed in clinical trials. You will also support preparation of regulatory documents in support of clinical trials.- In addition, you will be the site ... lead for the DAGS function at San Diego and will have oversight of the biospecimen operations and biobanking. You will serve as a strategic partner to our discovery… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …at each phase of the development are scientifically sound, can fulfill regulatory requirements and deliver the pre-specified product profile.CRO / Vendor ... Oversight : Review CRO/vendor proposal and budget. Establishes procedures through regular interaction, setting expectation on deliverables and timelines to guide CRO… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... organization. From health-care-provider interactions and developing and implementing regulatory strategies with the FDA to providing medical education and collecting… more
- Merck & Co. (North Wales, PA)
- …is based out of Upper Gwynedd, PA and will report to the Director , US Vaccines Contracting and Customer Experience within the C&DS organization. Responsibilities ... commercial programs.Maintains working knowledge of promotional review systems and regulatory guidance to effectively deliver compliant assets/programs.Manages the release… more
- Premera Blue Cross (Mountlake Terrace, WA)
- …Ethics & Regulatory Affairs team. This ** Director of Regulatory Compliance and Third-Party Oversight ** will work proactively to develop, enhance, ... oversight program and associated compliance committees and activities. + Provide oversight of Premera's regulatory advocacy efforts and relationship building.… more
