- Sumitomo Pharma (Boston, MA)
- …seeking a dynamic, highly motivated, and experienced individual for the position of ** Associate Director , Regulatory Affairs (Oncology).** The Associate ... with colleagues, fostering collaboration, and idea sharing + Reviews nonclinical, clinical and CMC documentation (eg nonclinical study reports, clinical … more
- Takeda Pharmaceuticals (Boston, MA)
- …in order to bring life-changing therapies to patients worldwide. Join Takeda as Associate Director , Global Labeling Lead where you will be responsible for ... develops and executes a labeling implementation plan to incorporate new scientific , safety and clinical data, as well as Health Authority responses / feedback… more
- Takeda Pharmaceuticals (Boston, MA)
- …employment application is true to the best of my knowledge. **Job Description** ** Associate Director , In Vivo Digital Portfolio & Data Stewardship** **About the ... Role** We are seeking an experienced ** Associate Director of In Vivo Digital Portfolio...of In vivo research with the ability to translate scientific and business needs into digital solutions that enhance… more
- Pfizer (Cambridge, MA)
- …on the reporting of clinical trial results to regulatory authorities and the scientific community by contributing to the clinical study reports, clinical ... **JOB SUMMARY** The **A** **ssociate** ** Director , Oncology Biometrics** is a skilled biostatistician who can work independently as the study statistician for Phase… more
- Bristol Myers Squibb (Devens, MA)
- …work and in their personal lives. Read more: careers.bms.com/working-with-us . The Associate Director Stability is responsible for stability product strategy and ... preparation, review and approval of stability reports and regulatory filings. The Associate Director is responsible for leading high-performance technical team,… more
- Sanofi Group (Framingham, MA)
- **Job Title:** Associate Director -CMC BioDPDM **Location** : Framingham, MA As Associate Director within CMC BioDPDM, you'll have the opportunity to lead ... could turn the impossible into possible for millions. The Associate Director role is a key leadership...development, process development, and tech transfer of programs to clinical and commercial manufacturing sites. + Bring a strong… more
- Sumitomo Pharma (Boston, MA)
- …seeking a dynamic, highly motivated, and experienced individual for the position of Associate Director , Market Access Engagement - Rare Disease, who will act ... + Develops and maintains a high-level, in-depth disease and therapeutic clinical and scientific knowledge + Utilize the CRM System to maximize efficiency and… more
- Takeda Pharmaceuticals (Boston, MA)
- …leadership at LOC level Decision-making and Autonomy + Responsibility in line with Associate Director level position; independently lead HE projects and support ... strategies for Health Technology Appraisal (HTA; including the EU Joint Clinical Assessment [JCA]) and payer assessments to optimize rapid, broad patient… more
- Takeda Pharmaceuticals (Boston, MA)
- …true to the best of my knowledge. **Job Description** **ABOUT THE ROLE** The Associate Director , GCP Audit & Compliance provides strategic quality oversight to ... clinical , medical, and pharmacovigilance suppliers across Takeda's global network....YOU BRING TO TAKEDA** + Bachelor's degree in a scientific , health, or medical field (or equivalent). + Minimum… more
- Lilly (Boston, MA)
- …Verve is headquartered in Boston, Massachusetts. **The Position** The purpose of the Associate Director , Regulatory Strategy role is to support the development ... subsidiary of Eli Lilly & Company within Lilly Research Labs, is a clinical -stage genetic medicines company established with a mission to solve the global health… more