- Gilead Sciences, Inc. (Foster City, CA)
- …Advertising and Promotion (RA Ad/Promo) is a core function within Gilead's Global Regulatory Affairs organization and acts as a critical strategic partner across ... + Experience working with external contractors supporting the work of regulatory affairs is a plus. + Experience authoring and/or implementing processes. +… more
- Gilead Sciences, Inc. (Foster City, CA)
- …of patients with life-threatening diseases. We have an exciting opportunity within US Medical Affairs for an Associate Director in our Patient Access and ... Director , Strategy Lead of PAQ Virology. The Associate Director of Medical Affairs ...the US healthcare landscape. + Solid working knowledge of regulatory and compliance environment. + Effective organizational, project planning,… more
- Gilead Sciences, Inc. (Foster City, CA)
- …opportunity to be based in our Foster City location. **Job Description** ** Associate Director , Global Medical Affairs (Primary Biliary Cholangitis)** ... This role is a leadership position within the Medical Affairs organization that reports to the Senior Director...meetings + Must be fully cognizant and adhere to regulatory and legal (Business Conduct) requirements for clinical trials… more
- Gilead Sciences, Inc. (Foster City, CA)
- …both medical and commercial disease and product training + Works with Executive and Senior Director , and Associate Director / Director on development of a ... Strategy - Liver Disease** Reporting to the Sr. Director US Medical Affairs (USMA) Liver Disease,...meetings. + Must be fully aware and compliant with regulatory and legal (Business Conduct) requirements for clinical trials… more
- AbbVie (San Francisco, CA)
- …*Position can sit in our Lake County, IL or Bay Area offices. Manager or Associate Director level depending on experience. The Associate Director ... collaboration with internal groups including Clinical Development and Operations; Epidemiology; Regulatory Affairs ; Medical Affairs ; Commercial; and Global… more
- BeiGene (Emeryville, CA)
- …clinical and clinical pharmacology sections of INDs, NDAs, BLAs, MAAs and other regulatory submission documents. The Associate Director , Medical Writing is ... **General Description:** The Associate Director , Medical Writing is responsible...of drug/biologics development, clinical research, study design, biostatistics, and regulatory affairs (eg, FDA and ICH guidelines… more
- BeiGene (Emeryville, CA)
- The Associate Director (AD) Clinical Study Management leads both indirect and direct reports, external partners, consultants, vendors and external budget to ... collaboration with functional area peers including Drug Safety, Quality Assurance and Regulatory Affairs , as well as thought leaders in order to meet program… more
- CSL Plasma (Hayward, CA)
- …Staff Associates for completion of training and recommendation for certification by Regulatory Affairs . Functionally directs the Center Medical Staff. Provides ... Usually serves as the primary center physician registered as the Laboratory Director with the Food and Drug Administration (FDA). **Job Description** + Serves… more
- Sutter Health (San Francisco, CA)
- …processes for GME activities Provides management support for Program Directors, Associate Program Directors, Core Faculty and residents / fellows. Collaborates with ... Program Directors and Associate Program Directors in setting programs' and short- and...with the Sutter Health GME's and ACGME's policies and regulatory requirements. Counsel's residents / fellows on program policies… more