- Pfizer (Cambridge, MA)
- …and external partners, such as project leaders, research units, biostatistics, regulatory affairs , clinical pharmacology, human genetics, translational ... Experience working with and solid understanding of related disciplines, eg, Clinical Operations, Safety, Biostatistics, Regulatory , Study Management, Pre-… more
- Pfizer (Cambridge, MA)
- …medicine, complemented by an extensive pipeline of over 50 programs in clinical development. + The Oncology Scientific Communications Director will report ... cross-functional input) with evolving evidence from clinical studies, insights, the Clinical Development Plan and regulatory strategy to ensure teams use… more
- Sanofi Group (Cambridge, MA)
- …Our Medical Affairs function serves as key strategic partners for commercial, regulatory , R&D, market access and external affairs to develop and launch first ... **Job Title:** Global LCM Senior Medical Director **Location:** Morristown, NJ Cambridge, MA **About the...the Job** This role is part of Global Medical Affairs team for Neurology within Specialty Care Medical … more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- …and external regulatory requirements. + Collaborate cross-functionally with Medical Affairs , Clinical Development, Regulatory , Legal, and Commercial ... The Senior Director , Medical Communications, CNS directs and provides strategic...and cross-functional teams (eg, Global Integrated Evidence & Innovation, Clinical Development, Regulatory , Commercial) to ensure global… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- …BU Lead and cross-functional teams (eg, Global Integrated Evidence & Innovation, Clinical Development, Regulatory , Commercial) to ensure global and US alignment ... **Job Summary** The Senior Director , Medical Communications, Nephrology & Immunology directs and...and alignment with the overall Nephrology & Immunology Medical Affairs strategy. The role is a key leadership position… 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**...Demonstrated industry experience working in strategic roles from medical affairs or clinical development related areas including… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- …report (FSR), including authoring statistical sections. + Discusses strategies with Global Clinical Development and Regulatory Affairs regarding study design ... for the maintenance of everyday health. As an Associate Director , Biostatistician, you will be a champion of Otsuka's...and key stakeholders across different functional areas such as clinical , regulatory affairs , asset management,… more
- Otsuka America Pharmaceutical Inc. (Waltham, MA)
- …other line functions including but not limited to Translational Research & Biomarkers, Clinical Management, Global Regulatory Affairs , Global Clinical ... on the early development CNS portfolio and Early Development Teams. This Senior Director is a strategic scientific and clinical leader accountable for the… more
- Sanofi Group (Cambridge, MA)
- …bring hope to patients with some of the highest unmet needs. Sanofi is recruiting a Director , US Medical Affairs . The Director will report to the Head of ... **Job Title:** US Medical Director , Dupilumab Atopic Dermatitis **Location:** Cambridge, MA /...At least 5 years of industry experience in Medical Affairs / Clinical Development is preferred, including significant experience… more
- Sanofi Group (Cambridge, MA)
- …Sclerosis, preferred. + Minimum of 4 years' experience in relevant Medical Affairs , research or clinical background + Demonstrated industry experience working ... **Job Title:** Global Medical Director **Location** : Cambridge, MA **About the Job**...in strategic roles from (global)medical affairs or clinical development related areas including… more