- Takeda Pharmaceuticals (Boston, MA)
- …is possible in order to bring life-changing therapies to patients worldwide. As an Associate Director, Global Regulatory Affairs Marketed Products you will ... area of regulatory strategy such as understanding broad concepts within regulatory affairs and implications across the organization and globally; proactively… more
- Veterans Affairs, Veterans Health Administration (Boston, MA)
- …stress and PTSD. 4. Prepares and ensures compliance with all research regulatory requirements. 5. Prepares and submits initial, ongoing, and final reporting ... research focused committees including editorial boards, grant review panels, and regulatory boards. 1. Academic/Teaching/Training (5% effort) - Will hold a faculty… more
- Takeda Pharmaceuticals (Lexington, MA)
- …of proposed promotional and disease state materials. + Collaborate with Regulatory Affairs , Medical, Legal, Commercial, and Compliance, execute and ... of my knowledge. **Job Description** Join Takeda as an Associate Director, US Advertising & Promotion Regulatory ... regulatory requirements. + Understand broad concepts within Regulatory Affairs and potential effects across the… more
- Takeda Pharmaceuticals (Boston, MA)
- …Regulatory Project Management and Strategic Planning - GI2 TAU within our Global Regulatory Affairs organization, based remotely. + Partners with the Global ... through proactive engagements with cross functional team members, Global Regulatory Affairs TAU colleagues and Global ...around the world. This position is currently classified as " remote " in accordance with Takeda's Hybrid and Remote… more
- Takeda Pharmaceuticals (Boston, MA)
- …area of regulatory strategy such as understanding broad concepts within regulatory affairs and implications across the organization and globally; proactively ... area of regulatory strategy such as understanding broad concepts within regulatory affairs and implications across the organization and globally; proactively… more
- Takeda Pharmaceuticals (Boston, MA)
- …FDA/EMA/PMDA regulations; ICH guidance; GLP/GCP requirements; SEND requirements, etc.). + Regulatory Affairs Credential (RAC-Drugs) is an advantage. + Strong ... to the best of my knowledge. **Job Description** **About the role:** ** Associate Director, Nonclinical Regulatory Writing and Submission Support,** **_Oncology… 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 ... and assures that Takeda labeling content and processes conform to regulatory requirements. Management of Local Exceptions and LOC Interactions + Manages… more
- Commonwealth Care Alliance (Boston, MA)
- …guidance, direction, and practical translation of privacy requirements (legal, regulatory , contractual and, as applicable, those emanating from national ... direct and indirect reports, and may have dotted line and/or regulatory /governance oversight responsibility of other relevant areas. **Supervision Exercised:** +… more
- CVS Health (Woonsocket, RI)
- …a hybrid working schedule of three days onsite per week and two days remote in one of the following locations: Woonsocket, RI, Hartford, CT, Irving, TX, Scottsdale, ... AZ, or Northbrook, IL As Associate Legal Counsel - Marketing, you will provide legal...Marketing, Privacy, Digital, Clinical, Corporate Communications, Compliance and Government Affairs . You will develop a deep understanding of business… more