- BeOne Medicines (San Mateo, CA)
- …medical affairs , and marketing. + Provide advice on healthcare regulatory matters across business functions, including commercial, clinical development, ... or health-related discipline, with at least 12+ years of experience in regulatory affairs , in advertising/promotion, labeling or related discipline + and 5 years… more
- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- **Job Description Summary** As Associate Director , Regulatory Affairs , you will be responsible for leading RA team members involved in device project ... Advanced degree preferred; medical training preferred. + Minimum 8 years of regulatory affairs experience within the pharmaceutical or medical device industries,… more
- Lilly (Indianapolis, IN)
- …to make life better for people around the world. Eli Lilly and Company seeks a Regulatory Affairs Director (R7-R8) to support the execution of regulatory ... followed by 5 years of progressively responsible experience with supporting regulatory affairs for pharmaceutical development projects and marketed products.… more
- Lilly (Indianapolis, IN)
- …new medicines to patients who need them all over the world. The Senior Advisor/ Director in Global Regulatory Affairs - CMC Pre-approval Small Molecules ... leverage CMC technical knowledge and regulatory science expertise to drive regulatory CMC strategies and develop submissions for clinical trials and… more
- Fresenius Medical Center (Waltham, MA)
- …(Advanced degree such as a Master's, PhD, or MBA is highly preferred). + Regulatory Affairs Certification (eg, RAC) is preferred. + **Experience:** + 12+ years ... regulatory submissions. + Collaborate with senior leadership in medical/ clinical development, commercial, and other functional areas to align...of experience in regulatory affairs , focusing on regulatory … more
- Stryker (San Jose, CA)
- The **Senior Director , Regulatory Affairs ** is a key strategist, responsible for developing regulatory strategy for the **Endoscopy business unit** and ... Canada and Europe. Through close partnership with business unit leadership, Marketing, R&D, Clinical and Quality teams, the Senior Director and team will develop… more
- Gilead Sciences, Inc. (Washington, DC)
- …directly relevant professional experience in small molecule and biologics development, global CMC regulatory affairs and CMC technical areas of at least 16 years ... an MA/MS, PhD, PharmD, or MD. + Demonstrated track record in leading CMC regulatory affairs initiatives, innovative CMC regulatory strategies, and leadership… more
- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- …product development, meet regulatory requirements, and support appropriate use. The Director of Medical Affairs needs to have strong strategic and ... directly to the business unit Vice President of Medical Affairs , the Director of Medical Affairs...interaction with cross functional development teams, and assessment of clinical evidence requirements to meet regulatory , safety… more
- Veterans Affairs, Veterans Health Administration (Brockton, MA)
- …and influence clinical and management decisions. b. Expert understanding of regulatory and quality standards for their program area. c. Ability to solve ... Summary This Clinical Pharmacy Specialist (Psychiatry) position is in the...medication therapy. As the PGY2 Psychiatric Pharmacy Residency Program Director , the incumbent manages all aspects of the residency… more
- Veterans Affairs, Veterans Health Administration (Tucson, AZ)
- …VA Health Care System (SAVACHS) is seeking a Physician to serve as the Clinical Director of the Cardiology Division. Commitment to excellence in patient care ... to the scientific literature is preferred. In addition to contributing to the clinical mission of the division, the division chief will be expected to participate… more
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