- Takeda Pharmaceuticals (Boston, MA)
- …Japan Payer Marketing and Market Access, Global Evidence and Outcomes, Medica Affairs , Clinical Development, Regulatory Affairs , Biostatistics, Global ... + Market Access, Pricing, Advocacy, Biostatistics, Global Evidence and Outcomes, Medical Affairs , Clinical Science, Legal, Regulatory + OBU 10, EUCAN, GEM… more
- Takeda Pharmaceuticals (Lexington, MA)
- …of my knowledge. **Job Description** About the role Join Takeda as an Associate Director, Medical Communications and Scientific Training (MCST) where you will be a ... other USBU Stakeholders; and Global functional groups such as Medical, Publications, Regulatory , Statistics, and Legal. * You will liaise with vendors for activities… more
- Takeda Pharmaceuticals (Lexington, MA)
- …of my knowledge. **Job Description** About the role: Join Takeda as an Associate Director, US Publications where you will work with Director, US Publications and ... and Global functional groups such as Medical, Publications, Medical Information, Regulatory , Statistics, and Legal. * Provide support to respective Product Medical… more
- Takeda Pharmaceuticals (Lexington, MA)
- …+ Serve as clinical liaison to Global Device Team, including engineering, regulatory affairs , quality, and commercial functions + Coordinate interdepartmental ... 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 Device… more
- Takeda Pharmaceuticals (Boston, MA)
- …assessment document + Engages with partner global functions (eg Clinical Science, Med Affairs , Regulatory Affairs , Biostats) to ensure alignment of global ... to shine? Join us as a PV Risk Management Scientist/ Associate Director. At Takeda, we are transforming the pharmaceutical...strive for excellence in everything we do. As an Associate Director/ PV Risk Management Scientist, being part of… more
- Merck (Boston, MA)
- …immunology, neurology, cardiometabolic and others as needed by the pipeline. + Work with Regulatory Affairs to ensure that regulatory documents (eg, IDEs, ... **Job Description** The Associate Vice President (AVP) / Companion Diagnostics will...stakeholders to ensure alignment with clinical development timelines and regulatory requirements. Most importantly, the role requires overseeing CDx… more
- Takeda Pharmaceuticals (Boston, MA)
- …to the best of my knowledge. **Job Description** **About the role:** The Associate Director, Clinical and Safety Quality Compliance is responsible for ensuring the ... and monitoring processes, and ensuring compliance with corporate and regulatory standards. By maintaining high-quality standards, this role supports Takeda's… more
- Takeda Pharmaceuticals (Boston, MA)
- …remote work allowed with 5 days/month onsite. **REQUIREMENTS:** Master's degree in Regulatory Affairs , Pharmacy, Biochemistry, Biology, or science related field ... job opportunity: **JOB LOCATION:** Cambridge, MA **POSITION** : Senior Research Associate **POSITION DESCRIPTION** : Takeda Development Center Americas, Inc. is… more
- Takeda Pharmaceuticals (Boston, MA)
- …provider's needs, enhance patient experience, and remain compliant with company and regulatory standards. As the Associate Director, Patient Services Operations, ... Marketing, Contracts and Pricing, Legal, Compliance, Training, Medical and Scientific Affairs and Regulatory , along with relevant external customers and… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …and policies. + Collaborate with internal cross-functional stakeholders (Marketing, PRT, Medical Affairs , Legal, Regulatory , Ethics & Compliance) to ensure the ... to the best of my knowledge. **Job Description** **About the role:** The Associate Director, Commercial Engagements & P2P Strategy, offers a unique opportunity to… more