- AbbVie (Chicago, IL)
- …the Medical Science Liaisons (MSLs) within a designated geographic region to achieve scientific and business objectives within a therapeutic area of US Medical ... Affairs . This includes, but is not limited to, coaching...process. + People Leadership and Development: Ultimate responsibility for scientific knowledge of self/team and oversight of MSL territory… more
- Pfizer (Cambridge, MA)
- …adoption of innovative trial designs while upholding the highest standards of scientific rigor and regulatory excellence. + **Team Leadership & Culture:** Inspire, ... + **External Engagement:** Act as a visible ambassador for Pfizer at scientific conferences, regulatory forums, and partner or investor engagements - articulating… more
- AbbVie (Mettawa, IL)
- …is a premier research group that has been widely recognized for its scientific expertise and leadership. Combining multiple scientific disciplines to generate ... cutting-edge evidence, the HEOR team supports AbbVie's scientific strategies and demonstrates the value of innovative treatments, shaping health care decision making… more
- J&J Family of Companies (Titusville, NJ)
- …Medicines and Device Development and Regulation, Program Management, Regulatory Affairs Management, Relationship Building, Safety-Oriented, Scientific Research, ... **Function:** Clinical Development & Research - Non-MD **Job Category:** Scientific /Technology **All Job Posting Locations:** Allschwil, Switzerland, Beerse, Antwerp,… more
- Xeris Pharmaceuticals, Inc. (Chicago, IL)
- …supporting Xeris' clinical programs. The individual will have a strong scientific background, exceptional writing skills, and a proven ability to translate ... complex clinical and scientific data into clear, accurate, and regulatory-compliant documents tailored to diverse audiences. **Responsibilities** + Develop and… more
- Mount Sinai Health System (New York, NY)
- …care policy. + A minimum of 5 years of research experience in Regulatory Affairs , Clinical Affairs or Quality Assurance with knowledge of Phase I-IV clinical ... development of investigator-initiated clinical trial protocols. Must understand complex scientific terminology and local, state, and federal regulatory requirements.… more
- Sanofi Group (Morristown, NJ)
- …a positive, collaborative mindset. + Take an active part in the scientific challenges involved in early clinical development, which require a scientifically ... (EDCO, including Clinical Trial Managers and Data Managers), Regulatory Affairs , Patients Safety & Pharmacovigilance, Therapeutic Area Research & Development… more
- Teva Pharmaceuticals (West Chester, PA)
- …responsibilities include statistical input to the evidence generation planning, medical affairs and RWE research proposal reviews, study protocol and statistical ... analysis plan (SAP) development and execution, results interpretation, scientific presentations and publications, interactions with agencies, and RWE/statistical… more
- Sanofi Group (Cambridge, MA)
- …could be critical in helping our teams accelerate progress. The Global Regulatory Affairs (GRA) Device team is a globally diverse team supporting the medical device, ... creates and maintains strong collaborative working relationships with Global Regulatory Affairs (GRA), Regional GRA, Country Regulatory Groups, Technical and Quality… more
- Merck (Boston, MA)
- …closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development projects; and ... company and competitors' drugs and internal and external expert opinion on scientific questions relevant to his/her areas of responsibility. **The Senior Director is… more