- Sanofi Group (Cambridge, MA)
- **Job Title:** Associate Director, Global Marketing, Hemophilia A (ALTUVIIIO & ELOCTATE) **Location:** Cambridge, MA **About the Job** Associate Director, Global ... on ex-US markets. Serve as key business partner for initiatives with corporate affairs . + Lead congress promotional activities for ALTUVIIIO + Serve as global… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …multiple projects, drive technical/scientific strategy and mentor junior engineers. The Associate Engineering Fellow will be leading complex programs and will be ... to effectively develop/ optimize/ scale-up and troubleshoot processes. The Associate Engineering Fellow will have experience with building scale-down equipment… more
- Rhythm Pharmaceuticals (Boston, MA)
- …learn, and our tenacity to overcome barriers, together. Opportunity Overview The Associate Director (AD) of Regulatory Operations is responsible for assisting the ... quality, accuracy, and adherence to regulatory guidelines. Additionally, the Associate Director supports the preparation and submission of Investigational New… more
- Takeda Pharmaceuticals (Boston, MA)
- …job opportunity: **JOB LOCATION:** Cambridge, MA **POSITION** : Senior Research Associate **POSITION DESCRIPTION** : Takeda Development Center Americas, Inc. is ... seeking a Senior Research Associate with the following duties: Manage the analytical release...with 5 days/month onsite. **REQUIREMENTS:** Master's degree in Regulatory Affairs , Pharmacy, Biochemistry, Biology, or science related field plus… more
- Bristol Myers Squibb (Cambridge, MA)
- …and in their personal lives. Read more: careers.bms.com/working-with-us . ** Associate Director, Global Regulatory Strategy, Neuroscience** **Position Summary:** The ... PhD, PharmD, BSN, etc.) with at least 3+ years of Regulatory Affairs experience in the pharmaceutical industry. **Key Competency Requirements** + Understanding of… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- ** Associate Director, Small Molecule Analytical Development** + Lead and oversee phase appropriate method development and optimization for drug substance and drug ... with analytical team members, process chemistry, formulation development, regulatory affairs , quality assurance, and other departments to drive scientific… 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 the ... at the Labeling cross functional teams including clinical, safety, medical affairs , and commercial, to ensure the highest level of communication effectiveness… more
- Takeda Pharmaceuticals (Boston, MA)
- …**Job Description** About the role: Join Takeda as a Regional Account Medical Lead ( Associate Director) where you will work with Account Management (AM) and serve as ... Takeda policies. .Lead effectively Field Medical Matrix partners (MSLs) and internal Medical Affairs experts to meet the need of key accounts for specialized or deep… 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 ... in GCP Quality/Compliance. + Advanced knowledge of pharmaceutical development, medical affairs and GCP/GVP regulations including FDA, EU, MHRA, PMDA and ICH.… more
- Takeda Pharmaceuticals (Boston, MA)
- …to the best of my knowledge. **Job Description** **About the role:** Associate Director, Clinical Program Quality Investigations is responsible for ensuring the ... in GCP Quality/Compliance. + Advanced knowledge of pharmaceutical development, medical affairs and GCP/GVP regulations including FDA, EU, MHRA, PMDA and ICH.… more