- Abbott (Santa Clara, CA)
- …clinical research and operational excellence? Join our high-impact team as a Senior Director , Clinical Study Management overseeing a global portfolio of 100+ ... Partnership: Serve as a strategic partner to the business by aligning clinical operations with long-term regulatory and reimbursement goals. Influence study… more
- Abbott (Pleasanton, CA)
- …Regulatory Affairs team within the Heart Failure Division (HFD) as the Global Director of Clinical Insights Development. This opportunity will report into the ... and resources) by working closely with internal stakeholders (R&D, Marketing, Clinical Affairs, Regulatory Affairs, Medical Affairs, Reimbursement ) and external… more
- Takeda Pharmaceuticals (Boston, MA)
- …the best of my knowledge. **Job Description** **About the role:** The Associate Director , Clinical & Quality Process Compliance is responsible for ensuring the ... process in partnership with functional compliance teams for regulations impacting Clinical , Safety and Clinical Pharmacovigilance Medical Quality (CPMQ)… more
- Philips (Cambridge, MA)
- As an important member of our talented Hospital Patient Monitoring (HPM) Clinical Affairs team, the Associate Director - Clinical Operations, is responsible ... day-to-day Clinical Operations/team Management and providing expertise in clinical research process legislation, ICH-GCP guidelines, improving efficiency in … more
- Philips (Cambridge, MA)
- …important member of our talented Hospital Patient Monitoring (HPM) CMO, the Clinical Development Portfolio Director is responsible for collaborating with ... multidisciplinary teams to deliver dynamic clinical evidence for Enterprise Hospital Monitoring & Cardio- New...match), HSA (with company contribution), stock purchase plan, education reimbursement and much more. Details about our benefits can… more
- Takeda Pharmaceuticals (Boston, MA)
- …will inspire you and empower you to shine? Join us as a Executive Medical Director , Oncology Clinical Sciences in our Cambridge office. At Takeda, we are ... Development Plan (IGDP). Responsible for review of synopses, other relevant clinical study documents and Critical Study Results. Provide leadership and oversight… more
- Pfizer (Collegeville, PA)
- …You will be responsible for scientific oversight, data integrity and quality of clinical trial(s) in support of the development strategy for programs within our ... Late-Stage Oncology portfolio. **KEY RESPONSIBILITIES** + Clinical development expert for assigned studies maintaining current scientific and clinical knowledge… 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 ... supports Takeda's mission by maintaining high standards of quality and compliance in clinical trials. **This role is located in Cambridge, MA and is Hybrid (not… more
- Marrakech, Inc. (Woodbridge, CT)
- …family, friends and acquaintances for their individual qualities and contributions. SUMMARY The Director of Clinical Services plays a vital leadership role in ... ensuring the coordination, oversight, and delivery of person-centered clinical services that support the overall health and well-being of individuals served by… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …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 ... highly innovative treatments to patients. These scientists (from quantitative clinical pharmacology, statistics, programming, outcomes research and epidemiology, patient… more