- Merck (Boston, MA)
- **Job Description** We are seeking a Director (Principal Scientist), Global Regulatory Affairs Liaison with a visionary, growth-oriented mindset that can ... drive our strategic priorities. The Director , Principal Scientist | Regulatory Affairs Liaison is responsible for development and implementation of… more
- Merck (Boston, MA)
- …Description** We are seeking a Senior Director (Sr. Principal Scientist) Global Regulatory Affairs Liaison with a visionary, growth-oriented mindset that ... **Summary, Focus and Purpose** The Senior Principal Scientist | Regulatory Affairs Liaison is responsible...external to GRACS. **Key Functions** + Reports to Executive Director or Associate Vice President, General Medicine + Works… more
- Merck (Boston, MA)
- **Job Description** The Regulatory Affairs Headquarters Principal Scientist is responsible for development and implementation of global regulatory strategy ... global regulatory point of contact on those projects within Global Regulatory Affairs and Clinical Safety (GRACS) and external to GRACS. + Develops worldwide… more
- AbbVie (Waltham, MA)
- …statistics, regulatory , etc ) as they relate to on-going medical affairs projects. May assist as consultant/ liaison with other corporations when working ... preferred. Will consider remote candidates. Purpose: The Associate Medical Director /Associate Scientific Director provides specialist medical/scientific strategic… more
- AbbVie (Cambridge, MA)
- …statistics, regulatory , etc.) as they relate to on-going medical affairs projects. + Experience in Neuroscience/Psychiatry preferred. + May assist as consultant ... be determined by the qualifications listed below. Purpose The Associate Scientific Director provides medical and scientific strategic and operational input into core… more
- Takeda Pharmaceuticals (Lexington, MA)
- …of proposed promotional and disease state materials. + Collaborate with Regulatory Affairs , Medical, Legal, Commercial, and Compliance, execute and ... my knowledge. **Job Description** Join Takeda as an Associate Director , US Advertising & Promotion Regulatory Review... regulatory requirements. + Understand broad concepts within Regulatory Affairs and potential effects across the… more
- Takeda Pharmaceuticals (Boston, MA)
- …of company Subject Matter Experts across Global R&D (Pharmaceutical Sciences, CMC Regulatory Affairs & Devices), Global Manufacturing Supply and Global ... true to the best of my knowledge. **Job Description** Senior Technical Regulatory Advisor - Pharmaceuticals (Senior/Executive Director ) OBJECTIVES/PURPOSE + To… more
- Veterans Affairs, Veterans Health Administration (Brockton, MA)
- …the purchase, fabrication or repair of prosthetic devices; Maintaining continuous liaison with manufacturers and dealers of prosthetic supplies, inspecting their ... at this level may serve as the (NCOPE) Residency Director for the site, or otherwise may be required...Conducts site surveys of commercial vendors to insure vendor regulatory compliance. Work Schedule: Monday - Friday, 8:00 am… more
- Sanofi Group (Boston, MA)
- …Marketing, Medical Affairs , Operations and Market Access. The Thought Leader Liaison , Rare Hematology will report to the Director , Thought Leader Liaisons, ... **Job Title:** Thought Leader Liaison - Rare Blood Disorders/Rare Hematology - Northeast...are on-label and consistent with commercial compliance, legal and regulatory guidelines. **KOL Development and Engagement** + Align with… more
- Takeda Pharmaceuticals (Boston, MA)
- …all applicable laws, regulations, and policies + Interact directly with Clinical, Statistics, Regulatory Affairs , and Medical Affairs to fully understand ... and be empowered to deliver your best. As part of the Global Medical Affairs Oncology team, you will report to the Scientific Communications Group Lead, Solid… more
- Novo Nordisk (Lexington, MA)
- …Clinical Operations, Non-Clinical Research, Medical Writing, Program Management, CMC and Regulatory Affairs teams. Will be interfacing with both internal ... to make a difference? The Position The International Medical Director serves as a subject matter expert for our...Operations, Non-Clinical Research, Medical Writing, Program Management, CMC and Regulatory Affairs teams to deliver and drive… more
- State of Massachusetts (Boston, MA)
- …records unit in filling these requests. * Assist the Director of External Affairs and the OCA Legislative Liaison in responding to inquiries from the ... Recreational Tramway Board and DOL's Warehouse program and its licensees. The Executive Director ("ED") will lead the administration and regulatory functions of… more
- Takeda Pharmaceuticals (Boston, MA)
- …the Regulatory Affairs CMC team, you will report to the Executive Director and Head, CMC Regulatory Affairs - Pharmaceuticals. **How you will ... bring life-changing therapies to patients worldwide. Join Takeda as a Senior Director , GRA CMC Pharmaceuticals Development Portfolio Lead where you will establish… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …Senior Management Cross-Functional Team (GLOC)** + In alignment with Head, Global Regulatory Affairs Marketed Products and Labeling, coordinates the process to ... patients with immunologic, hematologic, and other complex diseases. The Director , Global Labeling Strategy Lead is a key role...Future Fit and Submission Excellence). + Acts as the liaison between the labeling team members and senior leadership… more
- Pfizer (Cambridge, MA)
- …with research project leaders and projects team members, including biostatistics, regulatory affairs , clinical pharmacology, clinical scientists and development ... **ROLE SUMMARY** The purpose of the Senior Director of Clinical Research role is to coordinate...timelines. The clinical study lead will be the primary liaison for investigators who have enrollment or extraordinary protocol… more
- Sanofi Group (Cambridge, MA)
- …team and internal partners such as clinical operations, translational medicine, regulatory affairs , biostatistics, drug discovery, drug safety, marketing + ... be critical in helping our teams accelerate progress. The Clinical Research Director (CRD), Immunology & Inflammation (I&I) Therapeutic Area is responsible for the… more
- Sanofi Group (Cambridge, MA)
- …team and internal partners such as clinical operations, translational medicine, regulatory affairs , biostatistics, drug discovery, drug safety, marketing + ... what you thought was possible. Ready to get started? The Clinical Research Director (CRD), Immunology & Inflammation (I&I) Therapeutic Area is responsible for the… more
- Tufts Medicine (Boston, MA)
- …to make a difference. We are seeking a dynamic and experienced Executive Director , Surgical Services to join our renowned flagship hospital. As a key member ... and budgeting for designated areas. This is a senior director level role that manages multiple teams responsible for...in the ambulatory setting + Serves as an effective liaison with Medical Staff Leadership and key management and… more
- Tufts Medicine (Boston, MA)
- The Department Executive Director provides administrative and financial leadership, oversight, and management of the Department of Administrative Director ... goals for the service line. 5. Collaborates with External Affairs to develop and carry out marketing and/or public...a medical service provider of choice. 6. Maintains effective liaison with a variety of staff and management in… more
- Beth Israel Lahey Health (Westwood, MA)
- …lives.** Job Profile Summary Reporting to the Assistant Vice President of Regulatory and Compliance, this position is responsible for leading and overseeing the ... of the overall 340B Program including split-billing activities. In a regulatory capacity, coordinates and assists in identifying and evaluating 340B issues… more