- Lilly (Indianapolis, IN)
- …for people who are determined to make life better for people around the world. Associate Director - Clinical Trial Foundations Purpose: The Associate ... on the strategies, integrations, and improvements for systems and capabilities. The Associate Director is responsible for collaborating with business partners to… more
- Lilly (Indianapolis, IN)
- …creative solutions to support communities through philanthropy and volunteerism. The Associate Director Clinical Development, Oncology independently leads ... quality, on time, and within scope and budget. The Associate Director consistently demonstrates leadership and influence...Understand the scope of work required to complete the clinical trial successfully. Monitor the status and… more
- Lilly (Indianapolis, IN)
- …Sr. Director - R&D Tech@Lilly - Clinical Design & Operations, the Associate Director - Clinical Design will have direct responsibility for overseeing ... Design, Clinical Central Services, Investigator Experience, Trial Capabilities, Finance, and Clinical Trial...line staff, and a large contingent of contractors. This Associate Director works with business and R&D… more
- Lilly (Indianapolis, IN)
- …who are determined to make life better for people around the world. Purpose: The Associate Director , CTF Clinical Results Systems (as part of Clinical ... processes and technology ▪ Knowledge of emerging IT capabilities used for clinical trial data management ▪ Capacity and workload management expertise ▪ Strong… more
- Lilly (Indianapolis, IN)
- …culture to ensure diverse voices/ideas are considered. + Serves as mentor for clinical development managers, clinical trial project managers and others ... clinical deliverables in support of submissions, inspections, and publications. The Clinical Development Program Lead reports to the Associate Vice President… more
- Otsuka America Pharmaceutical Inc. (Indianapolis, IN)
- …translational clinical research experience (as a general guideline, 1-3 years for Associate Director level; 3-6 years for Director is typically required ... While not essential, prior personnel management experience, will support position at entry ( Associate Director / Director ). + An advanced understanding of drug… more
- Otsuka America Pharmaceutical Inc. (Indianapolis, IN)
- …academic translational clinical research experience (as a general guideline, 1-3 years for Associate Director level; 3-6 years for Director and 6-9 years ... While not essential, prior personnel management experience, will support position at entry ( Associate Director / Director ). + An advanced understanding of drug… more
- Merck (Indianapolis, IN)
- …component of decision-making at our company, this position offers an opportunity for the Associate Director to drive pipeline impact across therapy areas. This ... Associate Director will work with scientists within...models, exposure response (ER) models, model-based meta analysis (MBMA), clinical trial simulations (CTS) and disease progression… more
- Sumitomo Pharma (Indianapolis, IN)
- …marketed products. + Conduct safety surveillance over product life cycle, reviewing clinical trial and post-marketing Individual Case Safety Reports (ICSRs), ... highly motivated, and experienced individual for the position of ** Associate Medical Director .** The Associate ...safety of clinical trials, including monitoring of clinical trial safety and laboratory data. +… more
- Lilly (Lebanon, IN)
- …develop innovative solutions to optimize manufacturing processes and increase capacity for clinical trial medicines, while also reducing costs and environmental ... impact. The Associate Director - LRL L&D Strategic Site Consultant will report to the Lilly Research Laboratories Learning and Development (L&D) Director … more
- Lilly (Lebanon, IN)
- …develop innovative solutions to optimize manufacturing processes and increase capacity for clinical trial medicines, while also reducing costs and environmental ... clinical supplies and will therefore construct a new campus to manufacture Clinical Trial (CT) Active Pharmaceutical Ingredient (API) to meet needs for an… more
- Lilly (Indianapolis, IN)
- …develop innovative solutions to optimize manufacturing processes and increase capacity for clinical trial medicines, while also reducing costs and environmental ... impact. The Associate Director Maintenance provides leadership and direction to the maintenance and reliability groups within the site engineering organization.… more
- Lilly (Indianapolis, IN)
- …trials located in Lebanon, IN. This facility is Lilly's largest investment in a clinical trial manufacturing capacity and is intended to provide APIs for current ... 2025 and 2026.** **Position Summary:** The Engineering and Computer Systems Quality Associate Director is responsible for leading the team providing Quality… more
- Lilly (Indianapolis, IN)
- …develop innovative solutions to optimize manufacturing processes and increase capacity for clinical trial medicines, while also reducing costs and environmental ... impact. The Associate Director Engineering Facilities/Utilities provides leadership and direction to the engineering team responsible for plant and environmental… more
- Bristol Myers Squibb (Indianapolis, IN)
- …team, RayzeBio aims to be the global leader in radiopharmaceuticals. **Summary** The Associate Director of Chemistry, Manufacturing & Controls (CMC) - Quality ... assigned. + Member of CMC Development Teams providing Quality (QA) input from pre- clinical to end of product life cycle including NDA filing, other market filings,… more
- Lilly (Indianapolis, IN)
- …and mentoring role. - The development, conduct and reporting of corporate/global clinical trial (s) in support of registration and commercialization of potential ... of physicians on the day-to-day medical operations of the trial and will report to the AVP/Medical Director...**Responsibilities:** The - Cardiometabolic Health - Incretin Outcome Trials Clinical Research Physician will play a critical role in… more
- Otsuka America Pharmaceutical Inc. (Indianapolis, IN)
- **Job Summary** Under the direction of the Director / Associate Director of Clinical Management, the Senior Clinical Study Manager is responsible for ... communication of any variances in budget forecast to the Director / Associate Director .** **Establish communication flow...trial (s), as assigned.** **Participates in ongoing review of clinical trial data focusing on data integrity,… more
- Lilly (Indianapolis, IN)
- …finalization of CMC documents for global regulatory submissions, including Clinical Trial Applications, Market Authorization Applications, post-approval ... to make life better for people around the world. **Purpose:** The Senior Director of Global Regulatory Affairs - CMC (GRA-CMC) leads and manages the scientific… more
- Lilly (Indianapolis, IN)
- …for people around the world. **CT Supply Planning Tech@Lilly - Product Manager, Associate Director ** **What You'll Be Doing:** R&D Tech@Lilly unites science with ... time. This role will report to Mohit Gupta, Sr. Director , Clinical Supply & Delivery (CS&D). **How...and implement the landscape vision, strategy, and roadmap for clinical trial product delivery technology, in alignment… more