- 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
- 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
- Merck (Boston, MA)
- …and solutions to the world. **Looking for someone with a growth mindset. The Director , Regulatory Affairs Liaison is responsible for:** + Developing ... **Job Description** Our Regulatory Affairs team bring new medical...but are not limited to:** + Reports to Executive Director or Associate Vice President, Therapeutic Area… 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)
- **Our Team:** The Global Regulatory Affairs Device team is a globally diverse team supporting the medical device, combination product, digital health and ... the Sanofi portfolio of products. The team is part of the Global Regulatory Affairs , Regulatory CMC and Device Department within Global R&D. **Position… 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
- Takeda Pharmaceuticals (Lexington, MA)
- …is true to the best of my knowledge. **Job Description** Join Takeda as an Associate Director , Scientific Trainer out of our Lexington, MA office. Where you will ... supported US Medical therapeutic areas. You will collaborate with Medical Affairs partners (US Medical Strategy, Publications, Medical Communications, and Field… more
- Takeda Pharmaceuticals (Lexington, MA)
- …is true to the best of my knowledge. **Job Description** The Associate Director , Clinical Research provides clinical project management and leadership ... program management experienced in leading cross-functional clinical programs within Medical Affairs , Clinical Research, Regulatory , CMC or other drug development… more
- Sanofi Group (Cambridge, MA)
- About the job - US Medical Associate Director , Respiratory **Our Team:** This position will report into the US Medical Immunology team which is a segment of the ... Medical Affairs Specialty Care organization. Our Medical Affairs ...serves as a valued strategic partner with Clinical, Commercial, Regulatory , and Market Access on therapeutic solutions to support… 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
- 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
- Merck (Boston, MA)
- …Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... regulatory filing, and publication. **Specifically, The Senior Clinical Director May Be Responsible For:** + Evaluating pre-clinical and translational work… more
- Sanofi Group (Cambridge, MA)
- …Medical and Tactical Plans. + In coordination with the Field Medical Training Associate Director , ensure MSLs have robust scientific knowledge and communication ... Immunology team which is a segment of the Medical Affairs Specialty Care organization. Our Medical Affairs ...serves as a valued strategic partner with Clinical, Commercial, Regulatory , and Market Access on therapeutic solutions to support… more
- Commonwealth Care Alliance (Boston, MA)
- …duties as assigned. **Secondary Responsibilities** + Contribute towards the overall Department Regulatory Affairs and Compliance infrastructure at CCA. + Promote ... **Why This Role is Important to Us:** Under direction of the Director of Internal Audit, the primary functions of this position are to: + Contribute towards the… more
- J&J Family of Companies (Boston, MA)
- …closely with leaders in R&D, Supply Chain, Life Cycle Management, Quality, Regulatory Affairs , Finance, Procurement, Packaging, Marketing, and other business ... these businesses. + The Manager will supervise contractor(s) and will report to the Associate Director , Product Stewardship, J&J MedTech. The base pay range for… more
- Fresenius Medical Center (Waltham, MA)
- …+ Work collaboratively on projects with other FME departments including Compliance, Regulatory Affairs , Clinical Services, the Medical Office, Global IP, and ... manufacturers, and related entities. Under the general supervision of an Associate General Counsel or his/her designee, the Fellow undertakes projects supporting… more
- Novo Nordisk (Lexington, MA)
- …of more experienced personnel. Relationships The Medical Writer (MW) reports to an Associate Director of Medical Writing. The MW is expected to develop ... personnel from Medical & Science, Clinical Pharmacology, Biostatistics, Clinical Operations, Regulatory Affairs , Global Safety, Data Management, and Non-clinical… more
- State of Massachusetts (Boston, MA)
- …success in nation-leading clean energy policy, the Renewable Energy Policy Analyst willassistthe Director and Deputy Director and work with the Division staff ... regional, and federal REC markets, NEPOOL-GIS, the Federal Energy Regulatory Commission (FERC), and ISO-NE. The candidate shoulddemonstrateknowledge and experience… more