- Merck (Boston, MA)
- …Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... including development strategy, study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication. **Specifically, the Senior Director… more
- ICON Clinical Research (Boston, MA)
- …compliance with ethical, legal, and regulatory standards in medical and safety monitoring activities. + Representing the Medical Affairs Department in ... Medical Director (Pulmonology) - US- REMOTE ICON plc is...development initiatives. + Providing operational oversight within the Medical Affairs Department as needed. **Your profile** + Medical degree… more
- State of Massachusetts (Boston, MA)
- …of Occupational Licensure (DOL), an agency within the Office of Consumer Affairs and Business Regulation (OCABR), protects consumers by making sure the professionals ... DOL also licenses and regulates the Office of Public Safety and Inspections (OPSI), and the Office of Private...to be approved for use in Massachusetts. The Executive Director ("ED") for the Unit reports to the Associate… more
- Takeda Pharmaceuticals (Boston, MA)
- …among functions represented at the Labeling cross functional teams including clinical, safety , medical affairs , and commercial, to ensure the highest level ... to bring life-changing therapies to patients worldwide. Join Takeda as Associate Director , Global Labeling Lead where you will be responsible for the development… more
- Takeda Pharmaceuticals (Boston, MA)
- … safety issues with other functional areas such as Clinical Development, Regulatory Affairs , Quality Assurance, Medical Affairs , Marketing, Manufacturing, ... and products. + Develop strategy for and lead preparation of responses to safety -related inquiries from regulatory agencies and ethics committees. + Ensure… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …Safety , Clinical Sciences, Outcomes, Digital Health, Pharmaceutical Sciences/Device, and Global Regulatory Affairs . + Advanced knowledge of regulatory ... company that will inspire you and empower you to shine? Join us as Director , Quantitative Clinical Pharmacology (QCP) Lead in our Cambridge, MA office. Our Data and… more
- Takeda Pharmaceuticals (Lexington, MA)
- …+ Serve as clinical liaison to Global Device Team, including engineering, regulatory affairs , quality, and commercial functions + Coordinate interdepartmental ... into technical requirements + Coordinate risk mitigation activities across clinical, regulatory , quality, and engineering functions + Perform safety reviews… more
- Sanofi Group (Cambridge, MA)
- …internal partners such as clinical operations, translational medicine, regulatory affairs , biostatistics, drug discovery, drug safety , marketing. + Advance ... **Job Title:** Clinical Research Director **Location** : Morristown, NJ Cambridge, MA **About the Job** Ready to push the limits of what's possible? Join Sanofi in… more
- Astrix Technology (Boston, MA)
- …+ Collaborate with cross-functional teams, including preclinical, clinical operations, and regulatory affairs , to integrate and execute clinical strategy. + ... **Senior Medical Director ** Clinical Boston, MA, MA, US Pay Rate...as medical lead and monitor, maintaining focus on patient safety and treatment efficacy. + Drive biomarker strategy, including… more
- Sanofi Group (Cambridge, MA)
- …internal partners such as clinical operations, translational medicine, regulatory affairs , biostatistics, drug discovery, drug safety , marketing + Advance ... **Job title** : Clinical Research Director , I and I, Pulmonology **Location:** Cambridge, MA **About the Job** Are you ready to shape the future of medicine? The… more