- Lilly (Indianapolis, IN)
- …offering the following positions:** + Global Regulatory Strategy + Global Regulatory Policy + Global Regulatory Affairs : Product Communications + ... to make life better for people around the world. The Visiting Scientist Fellowship is a one-year postgraduate program that introduces participants to various… more
- Lilly (Indianapolis, IN)
- …to patients who need them all over the world. The Senior Advisor/Director Post approval scientist in Global Regulatory Affairs - CMC commercial solid oral ... strategies and submissions for Lilly's commercial solid oral products. The regulatory scientist will be encouraged to demonstrate innovative regulatory… more
- Lilly (Indianapolis, IN)
- …new medicines to patients who need them all over the world. We are seeking Regulatory Scientist GRA CMC-Parenteral Commercial Products to be a part of the Lilly ... tactical, and operational support for market registrations and post-approval submissions. The regulatory scientist will leverage CMC technical knowledge and … more
- Lilly (Indianapolis, IN)
- …medicines to patients who need them all over the world. The Advisor Post approval scientist in Global Regulatory Affairs - CMC Commercial Products will ... regulatory strategies and submissions for Lilly's commercial products. The regulatory scientist will be expected to demonstrate innovative regulatory… more
- Lilly (IN)
- …"patient journey" and the strategic plan for the compound), medical support for regulatory affairs and interactions with government agencies (medical support for ... drug discovery Drug/clinical development experience (for example, epidemiology, toxicology, pharmacology, regulatory affairs , medical affairs ) If experience… more
- Lilly (Indianapolis, IN)
- …who need them all over the world. The Senior Advisor/Director in Global Regulatory Affairs - CMC Pre-approval Small Molecules will leverage CMC technical ... the synthetic molecule portfolio, including small molecules, peptides, and oligonucleotides. The regulatory scientist will be expected to leverage innovative … more
- Lilly (Indianapolis, IN)
- …GPS organization, and with cross-functional teams including Statistics, Clinical Development, Regulatory Affairs , and others. **Global Patient Safety** GPS works ... the practice of pharmacoepidemiology?** We are seeking an ambitious post-doctoral scientist with strong research and communication skills, to contribute to an… more
- Lilly (Indianapolis, IN)
- …(PV) + Experience in defined functional business areas, for example, medical writing, regulatory affairs , or clinical trial management. + Knowledge of quality ... the development and maintenance of IT systems as the representative of MQO, Regulatory Quality. + Partner with IT and the business on system related… more
- Sumitomo Pharma (Indianapolis, IN)
- …but not limited to, Clinical Development, Translational Medicine/Early Development, Regulatory Affairs , Data Management and Biostatistics is essential. ... highly motivated, and experienced individual for the position of Pharmacovigilance Scientist to perform PV activities for assigned programs(s). Ability to work… more
- Grifols Shared Services North America, Inc (Indianapolis, IN)
- …and unmet needs within the therapeutic areas + Serves as an information scientist and colleague to top level academic physicians and researchers, select academic ... + Adheres to company policies and complies with applicable regulatory and legal requirements with highest ethical standards Skills/Qualifications/Education: (To… more