- Daiichi Sankyo, Inc. (Bernards, NJ)
- …by leveraging our world-class science and technology. With more than 125 years of scientific expertise and a presence in more than 20 countries, Daiichi Sankyo and ... centered around rare diseases and immune disorders. Summary: Responsibility for regulatory strategy to support the development of biomarkers, companion diagnostic… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …by leveraging our world-class science and technology. With more than 100 years of scientific expertise and a presence in more than 20 countries, Daiichi Sankyo and ... working with contract manufacturing organizations CMO. This position serves as the Regulatory Affairs (RA) CMC project representative to the CMC sub team and… more
- Merck & Co. (Durham, NC)
- …to ensure a successful Validation support of the vaccine manufacturing facilities.The Associate Director , Validation will be responsible for providing Validation ... biggest investors in Research & Development.We are seeking individuals with strong scientific and technical skills to contribute to the design, development and… more
- Eisai, Inc (Exton, PA)
- …coaches, and develops staff to maximize individual potential and to grow and retain scientific talent.The Associate Director is primarily responsible for the ... Quality Control, Regulatory , and CMC Program Management departments.The Associate Director of Biologics Operations maintains knowledge of established… more
- Genmab (NJ)
- …readiness, regulatory compliance, and successful data submissions.The Associate Director will lead cross-functional collaboration, provide oversight ... feel like a fit? Then we would love to have you join us!The RoleThe Associate Director , External Data Quality Management, is a strategic leadership role within… more
- Merck & Co. (Boston, MA)
- …development strategy, study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication.Specifically, the Senior Director ... and manufacturing to manage clinical development projects; and assist the Executive Director and/or Associate Vice President in ensuring that appropriate… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …research areas centered around rare diseases and immune disorders. Summary: The Associate Director , Laboratory Data Management is accountable for the end-to-end ... science and technology. With more than 125 years of scientific expertise and a presence in more than 20...of laboratory data for clinical trials, clinical development, and regulatory submissions. This position develops and proposes strategies for… more
- Merck & Co. (Rahway, NJ)
- …(as a lead GCS Planning program representative) such as clinical development, regulatory , quality and other supply chain areas to negotiate timelines,- strategies ... Ethics & Integrity. - Required Experience and Skills:- - Bachelor's degree in a scientific , business, or related discipline required , MS/MBA preferred . - At least… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …by leveraging our world-class science and technology. With more than 125 years of scientific expertise and a presence in more than 20 countries, Daiichi Sankyo and ... will collaborate globally with Formulation and Analytical Scientists, Clinical Operations, Regulatory Affairs CMC, and Clinical Development to collate the necessary… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …by leveraging our world-class science and technology. With more than 125 years of scientific expertise and a presence in more than 20 countries, Daiichi Sankyo and ... complexity in design and geographic scope). Prepares clinical section of regulatory document. Collaborates as team member with AROs/CROs. Drafts development plans,… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …by leveraging our world-class science and technology. With more than 125 years of scientific expertise and a presence in more than 20 countries, Daiichi Sankyo and ... effective vendor programming implementation, and expedite the preparation of regulatory submissions. Responsibilities include: make strategic programming decision and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …by leveraging our world-class science and technology. With more than 125 years of scientific expertise and a presence in more than 20 countries, Daiichi Sankyo and ... at each phase of the development are scientifically sound, can fulfill regulatory requirements and deliver the pre-specified product profile.CRO / Vendor Oversight:… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …by leveraging our world-class science and technology. With more than 125 years of scientific expertise and a presence in more than 20 countries, Daiichi Sankyo and ... areas centered around rare diseases and immune disorders. JOB SUMMARYThe Senior Director , Head Medical affairs Quality Assurance in Global RD/PV QA is accountable… more
- Kemin Industries (Des Moines, IA)
- Overview Kemin Health is hiring an Associate Director of Regulatory / Scientific Affairs and Quality! In this role, you will be responsible for leading the ... to support the overall strategic plan + Work cross-functionally and provide regulatory , scientific and quality expertise and support through all stages… more
- University of Washington (Seattle, WA)
- …at the WaNPRC, maintain regulatory compliance, and support cutting edge research.The Associate Director of Animal & Scientific Resources has broad ... National Primate Research Center (WaNPRC) has an outstanding opportunity for a **full-time Associate Director of Animal and Scientific Resources.** The… more
- Takeda Pharmaceuticals (Boston, MA)
- …development of scientific communications strategy and deliverables, the ** Associate Director , Scientific Communications Lead, Hematology** proactively ... background, preferably in life sciences, and excellent project management skills. The Associate Director , Scientific Communications Lead, develops and… more
- AbbVie (Mettawa, IL)
- …LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description Purpose The Scientific Director , US Medical Affairs provides specialist medical and ... relate to on-going medical affairs projects. Serves as the scientific team interface for key regulatory discussions....as the scientific team interface for key regulatory discussions. + Provide scientific /medical education to… more
- AbbVie (Mettawa, IL)
- …and LinkedIn. Job Description Key Responsibilities + Provide medical and scientific strategic input into core medical affairs activities, including interactions with ... Education & Experience Must have a PhD in a scientific field, & 3 years of work experience aligning...design and execution, including design of protocols, utilizing methodology, regulatory requirements governing clinical trials; & + consulting &… more
- ThermoFisher Scientific (Middleton, WI)
- …position located in either Middleton, WI or Richmond, VA** At Thermo Fisher Scientific , you'll discover meaningful work that makes a positive impact on a global ... strategies. + Conduct regular audits and reviews to ensure compliance with regulatory requirements. + Provide mentorship and guidance to team members, encouraging an… more
- BeOne Medicines (Emeryville, CA)
- **Position Summary:** The ** Associate Director , Statistical Programming** is responsible for leading a statistical programming team who supports multiple drug ... analysis requests, data validation, etc. in accordance with all relevant statistical regulatory guidance and standards. + Be a technical resource for programming… more
