- Lilly (Indianapolis, IN)
- …determined to make life better for people around the world. **Job Description:** The Clinical Data Scientist is responsible for developing and implementing ... data flow, and data standards. The Clinical Data Scientist collaborates with...data review solutions, dashboarding and analytics for a trial or set of trials within therapeutic… more
- Lilly (Indianapolis, IN)
- … Research/ Trial / Execution and Support + Participate in medical review of clinical trial data to ensure comprehensiveness, accuracy and validity of ... participates in: the development, conduct and reporting of corporate/global clinical trials in support of registration and...according to guidelines above. + Participate in reporting of clinical trial data in … more
- Merck (Indianapolis, IN)
- …drug approaches by leveraging QSP models to design and prioritize combination clinical trials + Broad understanding of population pharmacokinetic models and ... engagers, bispecifics) in Oncology, authoring regulatory documents (investigational new drugs/INDs, clinical study reports (CSRs), clinical trial … more
- Merck (Indianapolis, IN)
- …translational PK/PD approaches, population pharmacokinetic models, exposure-response models, clinical trial simulation, disease progression models, quantitative ... and biologics in Oncology, authoring regulatory documents (investigational new drugs/INDs, clinical study reports (CSRs), clinical trial applications… more
- Lilly (Indianapolis, IN)
- …position presents an opportunity to lead CMC activities to support clinical trials and regulatory submissions of peptide/oligonucleotide therapeutics. Developing ... needs across the rapidly evolving portfolio of medicines. The scientist will collaborate with a growing team comprised of...Regulatory) to implement and deliver material and information for clinical trials and regulatory submissions. + Design… more