- Takeda Pharmaceuticals (Boston, MA)
- …strong scientific and analytical background, preferably in life sciences, and excellent project management skills. The Associate Director, Scientific ... and discuss complex medical and scientific data + Understanding of pharmaceutical clinical development and product life-cycle management , clinical trial… more
- Sumitomo Pharma (Boston, MA)
- …a dynamic, highly motivated, and experienced individual for the position of ** Associate Director, Regulatory Affairs (Oncology).** The Associate Director is part ... (HA) information requests. In addition, this position may represent GRA in project related meetings, develop regulatory strategy and provide regulatory input as… more
- Sanofi Group (Cambridge, MA)
- …software development lifecycle, design controls, labeling, software documentation, risk management , clinical evaluations, and usability. Ability to synthesize ... **Job Title:** GRA Device Lead ( Associate Director) - Digital Health **Location:** Cambridge, MA/...GRA Device Lead for DHTs and SaMDs on assigned project teams (early phase, late stage and marketed products)… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- …with study team and key stakeholders across different functional areas such as clinical , regulatory affairs, asset management , safety and clinical operation. ... needs and nutraceutical products for the maintenance of everyday health. As an Associate Director, Biostatistician, you will be a champion of Otsuka's culture and… more
- Huron Consulting Group (Boston, MA)
- …environments + Proven ability to lead complex analytical workstreams with strong project management , client communication, and strategic problem-solving skills + ... Health systems, hospitals and medical clinics are under immense pressure to improve clinical outcomes and reduce the cost of providing patient care. Investing in new… more
- Sanofi Group (Cambridge, MA)
- **Job Title:** GRA Device Associate **Location:** Cambridge, MA/ Morristown, NJ/ Washington DC **About the Job** Are you ready to shape the future of medicine? The ... and Manufacturing & Supply, Regulatory Health Authorities, and others. As GRA Device Associate in the GRA Device Digital and Diagnostic team you'll contribute to… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- …for project quality + Exceptional ability to interpret complex clinical and scientific data and apply it consistently and accurately across communication ... The Associate Director, Scientific Communications manages the execution of...and cross-functional teams (eg, Global Integrated Evidence & Innovation, Clinical Development, Regulatory, Commercial). **Content Execution Direction** + Provide… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- …Quality Systems for managing the batch record review and release process Quality Management Activities supporting all phases of clinical development as well as ... **Job Summary** The Associate Director, Global Product Quality - Biologics is...- Biologics is responsible for directing quality oversight of clinical and commercial products at CMOs under contract by… more
- Bristol Myers Squibb (Devens, MA)
- …and in their personal lives. Read more: careers.bms.com/working-with-us . The Associate Director Stability is responsible for stability product strategy and ... with product stability strategy, stability program requirements, stability sample management , preparation, review and approval of stability reports and regulatory… more
- Baystate Health (Springfield, MA)
- …in healthcare quality and safety, is looking for a Part Time Operations Associate /Cardiac Monitor Technician to join our team in Springfield, MA.** **SCHEDULE:** + ... records. Facilitates communication among staff, relaying messages/information. Facilitates bed management and patient throughput on unit. Performs functions necessary… more