- Mount Sinai Health System (New York, NY)
- …a diverse portfolio of agreements and contracts in the support of the research activities of ISMMS Faculty. The ideal TTA candidate is reliable, motivated, ... priorities. The TTA works in partnership with MSIP Business Development team, all ranks of the ISMMS Faculty, and...and become the new standard of care **Qualifications** + PhD or JD, preferred + If JD, licensed to… more
- IQVIA (Albuquerque, NM)
- …May explore and identify sites for clinical trials in all stages of development . Incumbents have a deep scientific and clinical education and experience. Within ... and working practices + Complies with all guidelines, policies, legal, regulatory , and compliance requirements + Ensures effective administrative management of… more
- USAA (San Antonio, TX)
- …model validation, model development , statistical analysis, and/or advanced quantitative research . + **Advanced degree (eg, Master's, PhD )** in a quantitative ... and 4 years of related work experience in model validation, model development , statistical analysis, and/or advanced quantitative research . + Experience driving… more
- Sanofi Group (Cambridge, MA)
- …with typically at least 6 years of pharmaceutical experience in clinical development , including experience with Biotech, pharma, Clinical Research Organizations ... the future of medicine? The race is on to speed up drug discovery and development to find answers for patients and their families. Your skills could be critical in… more
- Henkel (Rocky Hill, CT)
- …timely commercialization. + Conceive and implement innovative approaches to product development using sound experimental design. + Present research findings ... all safety and regulatory standards. + Contribute to the technology roadmap, research publications, and IP strategy. **What makes you a good fit** + Master's or… more
- J&J Family of Companies (Raritan, NJ)
- … regulatory inspections, and health authority questions. **Qualifications:** + PhD in Chemical Engineering, Microbiology, Cell Biology, or related with 10+ ... safety management, and site escalations. In this capacity, they contribute to the development of robust strategies that maintain the validated state of cell therapy… more
- Kelly Services (South San Francisco, CA)
- …with expertise in statistical programming and data analysis to support clinical development and research initiatives. This individual will lead efforts in ... clinical study reports, and publications. * Act as programming lead for regulatory deliverables, ensuring alignment with ICH, FDA, EMA guidance, and internal… more
- AbbVie (North Chicago, IL)
- … advances and integrate this knowledge into Clinical Pharmacology strategy for research or development programs Responsibilities + Contribute to clinical ... to guide study design, and clinical pharmacology strategy. + Author regulatory documents including analysis plans, study reports, population PK reports,… more
- Danaher Corporation (Washington, DC)
- …ideas into impact - innovating at the speed of life. We're accelerating the development of cutting-edge diagnostics to solve some of the world's most pressing health ... with top academic institutions and leading players in biopharma and translational research . We're bringing the best minds together to accelerate innovation and… more
- Boehringer Ingelheim (Ridgefield, CT)
- …relevant internal global functions (eg Epidemiology, early and late-stage Clinical Development teams, Regulatory Affairs, Drug Safety, Marketing, PPSS (Product ... an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development and delivery of our products to our patients and customers. Our… more