- Otsuka America Pharmaceutical Inc. (Boston, MA)
- …the Senior Director to ensure timely and compliant submission of high- quality abstracts, posters, and manuscripts in line with Good Publication Practices (GPP) ... The Associate Director , Scientific Communications manages the execution of the...accurate, evidence-based, and compliant with internal policies and external regulatory requirements. + Collaborate cross-functionally with Medical Affairs… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- The Associate Director , Congress and Medical Education Strategy & Execution is responsible for executing and contributing to the global medical strategy and tactical ... through deep scientific understanding and collaborative partnerships. The Associate Director partners closely with global and regional cross-functional stakeholders… more
- Takeda Pharmaceuticals (Boston, MA)
- …to the best of my knowledge. **Job Description** **About the role:** Associate Director , Clinical Program Quality Investigations is responsible for ensuring the ... in GCP Quality /Compliance. + Advanced knowledge of pharmaceutical development, medical affairs and GCP/GVP regulations including FDA, EU, MHRA, PMDA and ICH. +… more
- Olympus Corporation of the Americas (Westborough, MA)
- …applicable federal, state or local law. Posting Notes: || United States (US) || Massachusetts (US-MA) || Westborough || Quality & Regulatory Affairs (QA/RA) ... + Minimum of 7 years experience managing the business aspects of quality and regulatory projects. + Good analytical toolkit. + Ability to influence outside of… more
- Sanofi Group (Cambridge, MA)
- …scientific exchange and engagement. We serve as key strategic partners for commercial, regulatory , R&D, market access and external affairs to develop and launch ... **Job Title:** Global Medical Director , Riliprubart **Location:** Cambridge, MA **About the Job**...of science to improve people's lives", Specialty Care Medical Affairs have a vision to be the leaders in… more
- Dana-Farber Cancer Institute (Attleboro, MA)
- In collaboration with the Senior Director of Network Operations, site Medical Director and Nurse Director , the Operations Director will oversee daily ... respect, sensitivity, confidentiality, and expert-based patient care delivery. The Operations Director will formulate and implement a plan for goals for the… more
- Sanofi Group (Cambridge, MA)
- **Job Title:** Global Medical Director **Location** : Cambridge, MA **About the Job** Join the team transforming care for people with immune challenges, rare ... strategy at the GBT level. + Participate and contribute to the Global Medical Affairs Strategic Plans for Frexalimab in line with key Strategic Imperatives. + Work… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- …statistical sections. + Discusses strategies with Global Clinical Development and Regulatory Affairs regarding study design and complex analysis issues, ... team and key stakeholders across different functional areas such as clinical, regulatory affairs , asset management, safety and clinical operation. + Familiar… more
- Sanofi Group (Cambridge, MA)
- …Research Director , Safety Officer and Pharmacovigilance, Translational Medicine, Regulatory Affairs , Biostatistics, Clinical Study Units, Medical Affairs ... **Job Title:** Development Scientific Director (DSD) **Location:** Cambridge, MA, **About the Job**...to the protocol development, study feasibility and risk assessment, regulatory submissions, protocol training, scientific review of data, and… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- …including INDs, IBs, clinical study reports, and NDAs/BLAs. + Collaborate with regulatory affairs on interactions with global health authorities. + Provides ... to post commercialization, with emphasis on the large global clinical trials and regulatory filing activities. The Senior Director , GCD is responsible for all… more