- Merck (North Wales, PA)
- …to study results transparency in the EU and US (in partnership with Regulatory Affairs) and submissions to CMS for price negotiations for certain products under ... balanced, and valuable to decision-makers (in partnership with V&I Outcomes Research ). * Training: Collaborates with internal stakeholders to determine the… more
- Capital One (Richmond, VA)
- …and at times defend state-of-the-art decision-making systems to internal and regulatory partners** + **Shape our practice of building machine learning models, ... from design through training, evaluation, validation, and implementation** + **Oversee development of benchmark and challenger models to stress test critical… more
- Pfizer (Seattle, WA)
- …(such as Medical Communications, Medical Affairs or scientific communications within Clinical Development roles). + Advanced scientific degree ( PhD , PharmD, MS, ... Communications within Pfizer Oncology Medical Strategy Management. + Leads development and execution of impactful scientific communication strategies for a… more
- J&J Family of Companies (Titusville, NJ)
- …acquire Intra-Cellular Therapies, Inc, a biopharmaceutical company focused on the development and commercialization of therapeutics for central nervous system (CNS) ... the VP, US Medical Affairs ITCI.** **Key Responsibilities:** + Lead the development of high-quality medical content to ensure clear, scientific communication of TA… more
- Lilly (Indianapolis, IN)
- …(DDCS) organization within Eli Lilly and Company supports the design, development , and commercialization of drug products and pharmaceutical delivery systems ... + Collaborate with formulation and analytical chemistry partners to perform mechanistic research and develop a robust understanding of key physical and chemical… 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
- 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