- Takeda Pharmaceuticals (Lexington, MA)
- … Affairs or related field, including 2+ years' experience specific to Regulatory Affairs - Advertising and Promotion. Candidates with experience in ... to address potential issues. **Accountabilities:** . Collaborate with colleagues in Regulatory Affairs , Medical, Legal, Commercial, and Compliance organizations… more
- Medtronic (Boston, MA)
- …own your future success. Together, we can transform healthcare. The Senior Director of Regulatory Affairs will lead the Regulatory team for Medtronic's ... potential acquisitions may also be required. This role reports to the Vice President, Regulatory Affairs for the Surgical Operating Unit and will be responsible… more
- Fresenius Medical Center (Waltham, MA)
- …for regulatory submission, including product labeling and promotional and advertising material. + Conducts regulatory intelligence as required for ... The ideal candidate should have US Advertising and Promotion experience. This position can be...fully remote. **PURPOSE AND SCOPE:** Ensures company products meet regulatory requirements by supporting all assigned regulatory … more
- Fresenius Medical Center (Waltham, MA)
- This position can be fully remote. **PURPOSE AND SCOPE:** Develops regulatory strategies for assigned products/product lines. Prepares regulatory submissions ... and systems designed to ensure the product development process addresses all regulatory requirements as well as the objectives of the business. **PRINCIPAL DUTIES… more
- Takeda Pharmaceuticals (Lexington, MA)
- … or related field, including a minimum of 2 years' experience specific to Regulatory Affairs - Advertising and Promotion. Candidates with experience in ... potential issues. **Position Accountabilities:** * Collaborate with colleagues in Regulatory Affairs , Medical, Legal, Commercial, and Compliance organizations… more
- Takeda Pharmaceuticals (Boston, MA)
- …sales, regulatory , legal, I&A, commercial operations, patient advocacy, medical affairs , and patient value and access. + Management of the product lifecycle. ... development of Core Visual Aid, Website, Key Opinion Leaders Videos, Digital Advertising etc. and routing of materials through the US Review Committee (USRC)… more
- Editas Medicine (Cambridge, MA)
- …articles, abstracts), and presentation materials. + Collaborate with Commercial, Legal, and Regulatory for development and review of labelling, advertising and ... the clinical pipeline. The incumbent is expected to have a strong clinical, regulatory and scientific foundation, and will work closely with the cross functional… more