- Takeda Pharmaceuticals (Boston, MA)
- …is possible in order to bring life-changing therapies to patients worldwide. Senior Associate - Specialist, Global Regulatory Affairs CMC role is within ... functions as follows: + With supervision, support the execution of regulatory CMC investigational, registration and post-approval strategies for assigned products. +… 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 ...if there is new data or campaigns that require senior level management input or alignment. + Strategic business… more
- United Therapeutics (Boston, MA)
- …or pharma regulatory experience with a Bachelor's Degree in life sciences, quality, regulatory affairs or a related area of study or 10+ years of biologic ... experience with a Master's Degree in life sciences, quality, regulatory affairs or a related area of...Ability to mentor, coach, guide, and train lower to senior level employees **Preferred Qualifications** + Proficient knowledge of… more
- Takeda Pharmaceuticals (Boston, MA)
- …of the Global Regulatory Affairs CMC team, you will report to the Senior Director Global Regulatory Affairs CMC. **How you will contribute:** + Plan, ... order to bring life-changing therapies to patients worldwide. Join Takeda as an Associate Director, GRA CMC Small Molecules where you will oversee the development… more
- Sanofi Group (Cambridge, MA)
- **Job Title:** Associate Director, Global Regulatory Affairs Advertising and Promotion **Location** : Cambridge, MA Morristown, NJ **About the Job** Are you ... thought was possible. Ready to get started? **Main Responsibilities:** + Represents Global Regulatory Affairs (US RA AdPromo) as a member of cross-functional… more
- Veterans Affairs, Veterans Health Administration (Leeds, MA)
- …social, and administrative data with guidance and instruction from supervisor or senior coder to develop knowledge of the organization and structure of an ... data to the national VA database. Identified data errors are reviewed with a senior coder or the supervisor and corrections made as directed. Uses a variety of… 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 ... for the following job opportunity: **JOB LOCATION:** Cambridge, MA **POSITION** : Senior Research Associate **POSITION DESCRIPTION** : Takeda Development Center… more
- Takeda Pharmaceuticals (Lexington, MA)
- …of my knowledge. **Job Description** **About the role:** Join Takeda as a Senior Manager, US Medical Information and Review where you will deliver high-quality, ... information / clinical expertise for assigned products to internal (Medical Affairs strategy teams, Therapeutic Area Units within R&D, commercial Brand teams)… more
- Takeda Pharmaceuticals (Lexington, MA)
- …Medical IISR clinical trials in assigned TA. Ensure coordination with Pharmacovigilance and Regulatory Affairs to respond to external audits and requests from ... Research and program management experience working with clinical programs within Medical Affairs , Clinical Research, Regulatory , CMC or other drug development… more
- Pfizer (Cambridge, MA)
- …design, conduct, and analysis. They work closely with other functions such as regulatory affairs , pharmacovigilance, biostatistics, and medical affairs to ... **Job Summary** The Senior Medical Director provides clinical development leadership and...the clinical development program meets the scientific, ethical, and regulatory standards. They also provides medical expertise and guidance… more