- Daiichi Sankyo, Inc. (Boston, MA)
- …experience in Oncology, clinical research and medical education preferred Principal MSL/ Associate Director MSL5 or More Years' experience including medical ... for cardiovascular diseases, under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily… more
- GRAIL (Boston, MA)
- …North Carolina, and the United Kingdom. It is supported by leading global investors and pharmaceutical, technology, and healthcare companies. For more information, ... Lab Operations, and other stakeholders to support regulatory strategy development, product validation, audits, promotional material review, on-market product … more
- Parexel (Boston, MA)
- **Job Purpose:** The Senior Clinical Research Associate (Sr. CRA) is responsible for the site management, site monitoring and close-out of assigned clinical trials ... within required timelines + Ensures adequate oversight of the investigational product at the investigator site, including receipt, handling, accounting, storage… more
- CSL Behring (Waltham, MA)
- …initiations, data releases, and product approvals, as guided by the associate director and working collaboratively with R&D and commercial teams. Contribute ... protect CSL's reputation and policy position. **Reporting Relationships:** **Reports to:** Associate Director , Corporate & External Affairs, R&D Portfolio **Main… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- **Job Summary** The Associate Director , Global Product Quality - Biologics is responsible for directing quality oversight of clinical and commercial ... processes, ensuring compliance with biologics-specific GMP requirements. This role has global responsibility for directing clinical and commercial product … more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- **Job Summary** The Associate Director Controlled Substances, Quality Global Product Quality - API/DP is responsible for directing quality oversight of ... with regulatory expectations and applicable cGMP/GDP quality standards. This role has global responsibility for directing clinical and commercial product quality… more
- Takeda Pharmaceuticals (Boston, MA)
- …the role:** As a Process Scientist ( Associate Director ) - Global Manufacturing Science GMSci Drug Product (DP), you will provide technical expertise ... Quality and Global Regulatory Affairs. + SME for Takeda drug product manufacturing organization and network. + In depth and broad understanding of drug … more
- Takeda Pharmaceuticals (Boston, MA)
- …the development of scientific communications strategy and deliverables, the ** Associate Director , Scientific Communications Lead, Hematology** proactively ... empowered to deliver your best. As part of the Global Medical Affairs Oncology team, you will report to...in life sciences, and excellent project management skills. The Associate Director , Scientific Communications Lead, develops and… more
- Sanofi Group (Cambridge, MA)
- **Job title** : Global Regulatory Affairs Device Lead ( Associate Director ) **Location** : Morristown, NJ or Cambridge, MA or Framingham, MA **About the Job** ... and global regulatory authorities to ensure compliance while optimizing product approval pathways. The team is accountable for developing and implementing … more
- Takeda Pharmaceuticals (Boston, MA)
- …and contribute to the company's success. These interfaces include but are not limited to Global Brand Teams (GBTs), Global Product Team (GPTs), Regional and ... leadership at LOC level Decision-making and Autonomy + Responsibility in line with Associate Director level position; independently lead HE projects and support… more
