- Otsuka America Pharmaceutical Inc. (Waltham, MA)
- …, Global Clinical Development (late phase), Data & Analytics, Early Commercial, Medical Affairs , Nonclinical Toxicology, Clinical Pharmacology, CMC, and Global ... to her/him on the early development CNS portfolio and Early Development Teams. This Senior Director is a strategic scientific and clinical leader accountable for… more
- Olympus Corporation of the Americas (Westborough, MA)
- …8 years medical device industry experience post-degree preferably in Clinical Affairs /Operations, Medical Affairs within biotech industry. + Experience ... protected by applicable federal, state or local law. Posting Notes: || United States (US) || Massachusetts (US-MA) || Westborough || Medical Affairs more
- Sanofi Group (Cambridge, MA)
- …with cross-functional teams, including Market Access Shared Services, Brand Strategy, Medical Affairs , Regulatory, Patient Support Services, distribution and ... **Job Title:** Value and Access - Dupixent Respiratory, Senior Director **Location:** Morristown, NJ Cambridge, MA **About...patients with some of the highest unmet needs. The Sr . Director of Access Strategy, Respiratory, is responsible for… more
- Edwards Lifesciences (Boston, MA)
- …and how our products transform patients' lives. As part of our Clinical Affairs team, you'll hone your scientific curiosity and passion for evaluating ... us and be part of our inspiring journey. The Senior Manager, Medical Writing oversees medical...expertise and collaborate with cross functional teams including Regulatory Affairs , Biostatistics, R&D, QA and Marketing on clinical data… more
- Takeda Pharmaceuticals (Boston, MA)
- …medicines and make a lasting impact on patients worldwide. Join Takeda as a Senior Director, Global Regulatory Lead - Oncology, where you will be part of the ... necessary, seeks expert advice and technical support from functional stakeholders and senior management. + Acts independently under the direction of a Global… more
- Takeda Pharmaceuticals (Boston, MA)
- …strategies in collaboration with their regional counterparts. **_Accountabilities:_** + The Senior Director will be responsible for complex or highly complex or ... project(s) of responsibility or oversees direct reports or other staff responsible. The Senior Director will lead all submission types. + Direct point of contact… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- …strategy, leading cross-functional study teams, and ensuring the highest standards of scientific and medical integrity. The incumbent will be responsible for ... proof of concept through late-stage trials and regulatory submissions. + Provide medical and scientific leadership to cross-functional study teams and ensure… more
- Merck (Boston, MA)
- **Job Description** ** Senior Principal Scientist Translational Medicine, Immunology** Translational Medicine in our Research & Development Division is responsible ... inflection point in the drug development process, working closely with scientific , regulatory, statistical, and modelling colleagues across the organization to… more
- Takeda Pharmaceuticals (Boston, MA)
- …represented at the Labeling cross functional teams including clinical, safety, medical affairs , and commercial, to ensure highly effective communication ... in order to bring life-changing therapies to patients worldwide. Join Takeda as Senior Manager, Global Regulatory Labeling Strategy where you will be responsible for… more
- Philips (Cambridge, MA)
- …important member of the Philips North America MRI Clinical Science team, the Senior MRI Clinical Scientist will collaborate with medical doctors and physicists ... large academic hospitals (most notably University of Texas Southwestern Medical Center) with a focus on research, development, and...or clinical application area, build a network in the scientific community and report and advise about new insights… more