- Catalent Pharma Solutions (Chelsea, MA)
- ** Associate Director , Regulatory Affairs ** **Position Summary:** Catalent is a global, high-growth, public company, and a leading partner for the ... safety of every patient, consumer and Catalent employee. The primary duty of the ** Associate Director , Regulatory Affairs ** is to support regulatory … more
- Sanofi Group (Cambridge, MA)
- About the Role The Associate Director , US Regulatory Affairs (RA) serves as the regulatory lead on relative Review Committees (RCs), for products in ... of prescription drugs and biologics. Essential Functions + Represents Global Regulatory Affairs (US RA AdPromo) as a member of cross-functional brand and… more
- Bausch Health (Boston, MA)
- …mission of improving people's lives with our health care products. he Associate Director , Advertising and Promotion, Prescription Drug Products, reviews, ... to enhance efficiencies and compliance. + Works closely with the Regulatory Affairs labeling group regarding package insert changes to assess and determine… more
- Sanofi Group (Cambridge, MA)
- The Associate Director RA serves as the regulatory lead on Review Committees (RCs). As the RC RA representative, work with brands on competitively ... + This individual is expected to competently and confidently represent Regulatory Affairs as a key member of cross-functional RC teams for assigned,… more
- Blue Cross Blue Shield of Massachusetts (Boston, MA)
- …you will work closely with the Vice President, State and Federal Government and Regulatory Affairs and other key leaders, including other division staff, to ... healthcare? Bring your true colors to blue. The Senior Director , Federal Government Affairs will manage BCBSMA...to the Vice President, State and Federal Government and Regulatory Affairs , and senior leaders including the… more
- AbbVie (Boston, MA)
- …Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description The Associate Director , RA Global Regulatory Strategy, US & Canada ... or Industry-related experience. + Preferred Experience: 5 years in pharmaceutical regulatory affairs . + Demonstrates effective communication skills in written… more
- Sanofi Group (Cambridge, MA)
- …pharmaceutical/biotechnology industry experience, including at least 4 years of relevant Regulatory Affairs experience (regionally and/or global) especially in ... **Main responsibilities:** + Leads the US regulatory activities. + As a key member of the Global Regulatory Team (GRT), and strategic partner to the Global … more
- Sanofi Group (Cambridge, MA)
- …pharmaceutical/biotechnology industry experience, including at least 4 years of relevant Regulatory Affairs experience (regionally and/or global) especially in ... team** The team is involved in developing and executing regulatory strategies for Tzield in life cycle development stages...a later diagnosis. **Main responsibilities:** + Leads the US regulatory post-marketing activities. + As a key member of… more
- Rhythm Pharmaceuticals (Boston, MA)
- …our tenacity to overcome barriers, together. Opportunity Overview As Associate Medical Director in North America Medical Affairs , you will contribute to the ... execution of the Medical Affairs strategy and tactics, assist with content development, KOL...a small, dynamic team and report to the Medical Director , North America. You will thrive in this role… more
- Sumitomo Pharma (Boston, MA)
- ** Associate Director , GMP Quality Control** Sumitomo Pharma America (SMPA) is focused on delivering therapeutic and scientific breakthroughs in areas of critical ... seeking a dynamic, highly motivated, and experienced individual for the position of Associate Director of GMP Quality Control, who oversees GMP compliance of… more
- Takeda Pharmaceuticals (Boston, MA)
- …in order to bring life-changing therapies to patients worldwide. Join Takeda as an Associate Director , Global Labeling Lead where you will be responsible for the ... will serve as the regulatory expert for labeling on the Global Regulatory Affairs subteam to ensure that regulatory labeling requirements are met for… more
- Sanofi Group (Boston, MA)
- The **Medical Science Liaison (MSL) Associate Director ** will oversee the effective and efficient functioning of individual MSLs in the region. Ideal candidate ... **Territory** : Western Region (West of Chicago) The **MSL Associate Director ** main objectives are to; +...material such as slide decks, in collaboration with Medical Affairs Directors. + Train or advise internal stakeholders. +… more
- Harvard University (Cambridge, MA)
- …Department Office Location:USA - MA - Cambridge Business Title: Associate Director for LicensureSub-Unit: Salary Grade ... of Education does not provide Visa sponsorship. Position Description: Associate Director for Licensure will oversee all...the licensure process. This role reports to the Senior Associate Dean of Academic Affairs and Student… more
- Sanofi Group (Cambridge, MA)
- …into the Global Medical Immunology team that is part of the Medical Affairs Specialty Care organization. Our Medical function serves as a key strategic partner ... with commercial, regulatory , clinical, and market access on therapeutic solutions to...solutions to support patients' needs. Within the Global Medical Affairs Immunology team, we are proud to support Sanofi's… more
- Sanofi Group (Cambridge, MA)
- …gastrointestinal diseases. **Main Responsibilities:** The Global Medical Immunology Pipeline Associate Director , Gastroenterology, reports to the Global Medical ... clinical care. We curate patient and scientific evidence and partner with commercial, regulatory , R&D, market access, and external affairs teams to develop… more
- Sanofi Group (Cambridge, MA)
- …Medical function serves as a valued strategic partner with Clinical, Commercial, Regulatory , and Market Access on therapeutic solutions to support patients' needs. ... patients. **Job Description:** This position reports to the Senior Medical Director , Respiratory/Allergy. Main job responsibilities: + In partnership with the… more
- Merck (Boston, MA)
- …colleagues, GCTO Country Operations, other GCTO functional areas, Pharmacovigilance (PV), Global Regulatory Affairs and Clinical Safety (GRACS), IT, etc.) is ... teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new drugs, vaccines and new indications for existing… more
- Integra LifeSciences (Mansfield, MA)
- …are challenging what's possible and making headway to help improve outcomes. The Associate Director , Instruments & Lighting Marketing role will have end-to-end ... including field sales, country marketing teams, product development, finance, regulatory , clinical/medical affairs , business development and others; demonstrates… more
- Takeda Pharmaceuticals (Lexington, MA)
- …product responsibilities. As part of the US Medical team, you will report to the Associate Director , Ad/Promo Regulatory Review. You will be based in either ... potential issues. **Position Accountabilities:** * Collaborate with colleagues in Regulatory Affairs , Medical, Legal, Commercial, and Compliance organizations… more
- Sanofi Group (Cambridge, MA)
- …study, compound, protocol + TA Experts, senior CRDS, global clinical lead, GPHs and medical affairs + CROs + Regulatory affairs + Collaborates with other ... **Clinical Research Director - allergy-immunology-dermatology** The Clinical Research Director...clinical study report + Take on as necessary the Associate CRD role: + Develop the abbreviated protocol +… more