- Roche (South San Francisco, CA)
- …new medicines to patients? We are seeking a Technical Regulatory Program Director to join our Pharma Technical Regulatory (PTR) department. This position plays ... Develop, communicate and implement robust regulatory strategies that align with global regulatory requirements + Identify and communicate regulatory risks; develop… more
- Citigroup (New York, NY)
- ** Director , Wealth Communications** The Enterprise Services and Public Affairs (ESPA) team's mission is to enhance how our internal and external stakeholders - ... of the firm, its businesses and the brand. The Global Communications team is an agile, high-impact group that...across the three businesses for Citi internal channels (Citi Global News, Citi Features, Citi Wealth Newsletter, etc.) +… more
- Lilly (Indianapolis, IN)
- …to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work ... for people around the world. **Role Overview** The Sr. Director , Clinical Development is an experienced clinical trialist who...be responsible for the clinical and scientific execution of global clinical programs. They will play a key role… more
- Takeda Pharmaceuticals (Boston, MA)
- …best of my knowledge. **Job Description** **About the role:** The Associate Director , Clinical and Safety Quality Compliance is responsible for ensuring the quality ... continuous improvement that are enterprise-wide (ie Veeva, QMS, Enterprise Audit, etc.) to Global Quality and R&D Quality. Present to CPMQ at periodic intervals the… more
- Charles River Laboratories (Wayne, PA)
- …more Charles River operations and serves as a member of the Regulatory Affairs and Compliance management team. Provides direction in implementing the Charles River ... applicable regulatory requirements. ⦁ Assume a key role in designated Regulatory Affairs and Compliance projects and programs. ⦁ Participate in Corporate Quality… more
- BeOne Medicines (Emeryville, CA)
- …Medical Writer to lead the tactical execution of publications stemming from our global medical affairs publication plans. These plans span across early phase ... outcomes research in the oncology space + Familiarity with global regulatory and medical affairs environments (eg, US, EU, APAC) + Experience with publication… more
- Bristol Myers Squibb (Madison, NJ)
- …patient/clinician reported measures across Cell Therapy portfolio. Support the Executive Director in developing and executing health economic & outcomes research ... Work as part of cross-functional teams-including clinical development, medical affairs , regulatory, and biostatistics-to ensure HEOR contributions are integrated… more
- Bristol Myers Squibb (Madison, NJ)
- …and in their personal lives. Read more: careers.bms.com/working-with-us . The Associate Director , MEG Lead Oncology will be responsible to support relationships with ... + At least 5 years of experience in pharmaceutical Medical Affairs , Clinical Development or relevant experience; previous customer-facing role experience highly… more
- Gilead Sciences, Inc. (Foster City, CA)
- …performance indicators, training, and scope/remit. + Successfully partner with Global Commercial, Medical Affairs , Business Conduct, Finance, Regulatory, ... Join Gilead and help create possible, together. **Job Description** The Director of US Commercial Congresses, within the Strategic Meetings & Engagements… more
- Gilead Sciences, Inc. (Foster City, CA)
- …Join Gilead and help create possible, together. **Job Description** **Associate Director , Competitive Intelligence - Breast Cancer** , will support CI activities ... one of Gilead's core oncology priorities. CI is a key function within Gilead's global organization and this role is a great opportunity to have broad visibility… more