- Sanofi Group (Cambridge, MA)
- …an innovative global healthcare company with one purpose: to chase the miracles of science to improve people's lives. We're also a company where you can flourish and ... of sanofi revenues by expediting submission timelines and facilitating reviews by regulatory agencies of sanofi key assets. + He/she: Creates and executes a… more
- Merck (Boston, MA)
- …development (MIDD) to routinely enable efficient drug discovery/development and/or regulatory decisions. The Pharmacometrics group within QP2 brings an experienced ... analyses + Developing and maintaining a comprehensive understanding of global regulatory expectations for small molecules and biologics, authoring regulatory … more
- Takeda Pharmaceuticals (Cambridge, MA)
- …in digital health, global outcomes/epidemiology, biostatistics, and other key data science disciplines. + Serves as an ambassador of Quantitative Clinical ... (eg, QSP, MBMA) to inform internal decisions and external regulatory interactions. + Represents Clinical Pharmacology in meetings with...AND SKILLS:** **Education & Experience** + Pharm D. or PhD with 8+ years of working experience in a… more
- Sanofi Group (Framingham, MA)
- …an innovative global healthcare company with one purpose: to chase the miracles of science to improve people's lives. We're also a company where you can flourish and ... for investigations and deviation resolution. + Work collaboratively with MSAT Process Science team, recommend changes and/or study plan to improve process robustness… more
- Sanofi Group (Cambridge, MA)
- …an innovative global healthcare company with one purpose: to chase the miracles of science to improve people's lives. We're also a company where you can flourish and ... compliance with all corporate and industry policies and legal and regulatory requirements, for all medical affairs activities + Ensure promotional/non-promotional… more
- Bristol Myers Squibb (Cambridge, MA)
- …. The **Clinical Scientist Program Lead** reports through the Clinical Science function which provides scientific expertise necessary to design and deliver ... of innovative protocols and data packages for CSRs and Regulatory Filings. The Program Lead oversees all clinical studies...program(s). * Serves as a member of the Clinical Science Leadership Team and Global Program Team * Drives… more
- Sanofi Group (Cambridge, MA)
- …**:** + A minimum of a Bachelor's Degree is required. MBA, MS or PhD in life science is preferred + **Extensive and diverse industry experience** ... products, understanding unmet needs, and connecting communities. We chase the miracles of science every single day, pursuing progress to make a real impact on… more
- Bristol Myers Squibb (Devens, MA)
- …fate/effects studies and environmental risk assessments according to appropriate international regulatory guidelines. This role will lead and participate on diverse ... risk assessments and environmental fate/effects studies focused on global regulatory frameworks, technical knowledge and emerging scientific trends; Lead matrix… more
- Charles River Laboratories (Shrewsbury, MA)
- …study management, interpretation, and reporting of study data and assuring the regulatory compliance of these projects, as appropriate. Serve as a Project Scientist ... protocols/plan in accordance with company standard operating procedures and industry regulatory guidelines. This position will serve as the primary scientific… more
- Charles River Laboratories (Shrewsbury, MA)
- …management, interpretation, and reporting of study data and assuring the regulatory compliance of these projects, as appropriate. Additional responsibilities include ... protocols/plan in accordance with company standard operating procedures and industry regulatory guidelines. This position will serve as the primary scientific… more