- Rhythm Pharmaceuticals (Boston, MA)
- …learn, and our tenacity to overcome barriers, together. Opportunity Overview In the Associate Director , Regulatory Affairs role, you will be responsible for ... commercialization and life cycle of Rhythm products. This role reports into the Director , Global Regulatory Affairs. Responsibilities and Duties + Act as the Global… more
- Takeda Pharmaceuticals (Lexington, MA)
- …is true to the best of my knowledge. **Job Description** **About the Role:** The Associate Director of Device Clinical Development (DCD) in the Drug Product and ... that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's… 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 ... application process with Takeda will commence and that the information I provide in my application will be processed...clinical, medical , and pharmacovigilance suppliers across Takeda's global network. You… more
- Philips (Cambridge, MA)
- …of our talented Hospital Patient Monitoring (HPM) Clinical Affairs team, the Associate Director - Clinical Operations, is responsible for day-to-day Clinical ... the updates and enhancement of quality system processes for Clinical & Medical Affairs, aligning with business strategies, roadmaps, and Informatics demands. +… more
- Guidehouse (Boston, MA)
- …time. + Authorized to work for any US employer without sponsorship. As an Associate Director + BA/BS degree in Science, Engineering, Healthcare, Business or ... 5-7 years of Life Sciences (Pharmaceutical, Biotech, Specialty Pharma and/or Medical Technology) consulting experience is required. Advanced degree (PhD, PharmD,… more
- Takeda Pharmaceuticals (Boston, MA)
- …true to the best of my knowledge. **Job Description** **About the role:** Associate Director , Clinical Program Quality Investigations is responsible for ensuring ... application process with Takeda will commence and that the information I provide in my application will be processed...and share insights to trends to Clinical Pharmacovigilance and Medical Quality and R&D Quality leadership for proactive risk… 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 ... application process with Takeda will commence and that the information I provide in my application will be processed...at the Labeling cross functional teams including clinical, safety, medical affairs, and commercial, to ensure the highest level… more
- Takeda Pharmaceuticals (Boston, MA)
- …to the best of my knowledge. **Job Description** **About the role:** The Associate Director , Clinical & Quality Process Compliance is responsible for ensuring ... that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- The Associate Director of Regulatory Intelligence leads the collection and dissemination of regulatory intelligence and collaborates with SMEs to interpret the ... have continued access to regulatory, clinical trial, and public domain information resources to identify relevant regulatory-related news and information ,… 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 ... and development to bring novel therapies to patients sooner. For more information on SMPA, visit our website https://www.us.sumitomo-pharma.com or follow us on… more