- Takeda Pharmaceuticals (Boston, MA)
- …is possible in order to bring life-changing therapies to patients worldwide. The Associate Director Global Regulatory Affairs, Neuroscience is responsible ... for developing innovative global regulatory strategies and providing strategic regulatory guidance...and Takeda R&D. **How you will contribute:** + The Associate Director will be responsible for increasingly… more
- Takeda Pharmaceuticals (Boston, MA)
- … strategies in collaboration with their regional counterparts. **Accountabilities:** + The Associate Director will be responsible for complex or highly complex ... needs and anticipates such changes to lead adaptations to regulatory strategy. + Ensures project team colleagues,...(s) of responsibility or oversees direct reports responsible. The Director will lead all submission types. + Accountable for… more
- 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 ... cycle of Rhythm products. This role reports into the Director , Global Regulatory Affairs. Responsibilities and Duties...Affairs. Responsibilities and Duties + Act as the Global Regulatory Lead on multi-disciplinary project teams and… more
- Takeda Pharmaceuticals (Boston, MA)
- …is possible in order to bring life-changing therapies to patients worldwide. The Associate Director , Global Regulatory Affairs Advertising and Promotion (GRA ... medicine promotion. **How you will contribute:** + As our Associate Director , Global Regulatory Affairs...and commercial materials. + You will be product or project business lead for global CMRP at Takeda +… more
- United Therapeutics (Boston, MA)
- …like lungs, pancreases and hearts. **Who you are** We are looking for a regulatory strategist who will advise on regulatory pathways, managing documentation and ... timelines, and supporting the preparation and execution of regulatory submissions for our whole organ tissue engineering program....a related area of study + 8+ years of project or people management experience + Must have written… more
- Boston University (Boston, MA)
- ** ASSOCIATE DIRECTOR , CONSTRUCTION & PROJECT SAFETY, Research Compliance** **Job Description** ** ASSOCIATE DIRECTOR , CONSTRUCTION & PROJECT ... 9/19/2025 **Salary Grade** Grade 50 **Position Type** Full-Time/Regular The Associate Director , Construction and Project ...position will provide sign off on design for all regulatory components, as well as performing routine site visits… more
- IQVIA (Boston, MA)
- **Position Overview:** IQVIA is seeking an experienced Associate Clinical Project Management Director /Trial Delivery Manager (TDM) to lead and coordinate ... and retention of trial documents. + Provide central documents for regulatory submissions. + Support Health Authority inspections and internal audits. **Training… more
- AbbVie (Waltham, MA)
- …with HEOR Strategy and other functions (eg, Clinical Development & Operations, Regulatory , Commercial). The Associate Director , Patient-Centered Outcomes ... research organizations, patient advocacy groups). The Associate Director represents HEOR at global regulatory and...matrix environments and on a global level + Excellent project management skills + Demonstrated experience / knowledge of… more
- Sanofi Group (Cambridge, MA)
- **Job Title:** GRA Device Lead ( Associate Director ) **Location:** Cambridge, MA/ Morristown, NJ **About the Job** Are you ready to shape the future of medicine? ... critical in helping our teams accelerate progress. The Global Regulatory Affairs (GRA) Device team is a globally diverse...Responsibilities** + Serve as GRA Device Lead on assigned project teams (early phase, late stage and marketed products)… more
- Bristol Myers Squibb (Cambridge, MA)
- …at work and in their personal lives. Read more: careers.bms.com/working-with-us . ** Associate Director , Global Regulatory Strategy, Neuroscience** **Position ... from HAs for respective regions/countries + Prepare content for regulatory strategic documentation and Regulatory Project Reviews. Align regulatory plans… more
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