- Sanofi Group (Morristown, NJ)
- …discipline, PharmD, or medically qualified with: + Min 15 years of experience working in clinical development and/or regulatory affairs + Min 10 years of ... **Job Title:** Clinical Documentation Global Head **Location** : Cambridge, MA,...revenues by expediting submission timelines and facilitating reviews by regulatory agencies of sanofi key assets. + He/she: Creates… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …through close collaboration with cross-functional teams (including Medical Affairs , Clinical Development, Regulatory Affairs , Commercial, GPD comms), to ... Expertise:** + Comprehensive understanding of the pharmaceutical industry and medical affairs + Global regulatory expertise with demonstrated strong ability… more
- Danaher Corporation (Boston, MA)
- …digital pathology in the clinical oncology environment. The Senior Principal, Regulatory Affairs will provide oversight and lead global submission work ... m (https://www.danaher.com/how-we-work/danaher-business-system) which makes everything possible. The Senior Principal, Regulatory Affairs is responsible for regulatory… more
- University of Pennsylvania (Philadelphia, PA)
- …participate in the coordination of Phase I-V clinical trials. Reporting to the Regulatory Affairs Research Teams Manager, the Regulatory Affairs ... programs and resources, and much more. Posted Job Title Clinical Research Regulatory Specialist B (Abramson Cancer...cutting-edge oncology treatments. Contingent upon funding. The ACC OCCR Regulatory Affairs Office seeks a full-time … more
- Sumitomo Pharma (Helena, MT)
- …for Oncology clinical development activities. + Partner with Translational Research, Regulatory Affairs , Clinical Operations, and Medical Affairs ... (including Clinical Operations), Biometrics, Regulatory , Early Clinical Development, Pre- clinical research, Medical Affairs and Commercial… more
- System One (Florham Park, NJ)
- …documents for electronic submissions. + Coordinate with cross-functional teams, including Regulatory Affairs , Clinical Development, and Quality Assurance, ... deadlines are met. + Ability to work collaboratively with cross-functional teams, including regulatory affairs , clinical operations, and quality assurance in… more
- Sanofi Group (Morristown, NJ)
- …methodologies. + Collaborate with glocal cross-functional teams including Medical TA, Clinical Development, Regulatory Affairs , HEVA, Market Access, ... engagement. We serve as key strategic partners for commercial, regulatory , R&D, market access and external affairs ...collaborate with internal experts from Global and Local Medical, Clinical Development, and Regulatory teams to develop,… more
- Gilead Sciences, Inc. (Santa Monica, CA)
- …in a team environment comprising clinical operations, biomarker specialists, CROs, and regulatory affairs . + Provide clinical expertise and input for ... boards, patient advocacy groups) and internal stakeholders (Research, Translational Sciences, Clinical Operations, Safety, Regulatory , Medical Affairs , and… more
- System One (Tarrytown, NY)
- …or aggregate report teams. + Collaboration with Signal Management, Medical Safety, Clinical , Regulatory Affairs , and Biostatistics groups. + Experience ... with Global Patient Safety (GPS) and with functional areas (Epidemiology, Clinical Development, Regulatory Affairs , Statistics, etc.) contributing… more
- Gilead Sciences, Inc. (Foster City, CA)
- …+ Work closely in a team with key cross functional partners including regulatory affairs , patient safety, clinical operations, biostatistics, clinical ... boards, patient advocacy groups) and internal stakeholders (Research, Translational Sciences, Clinical Operations, Safety, Regulatory , Medical Affairs , and… more
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