- Lilly (Indianapolis, IN)
- …and information to enable clinical development and speed medicines to patients. The Associate Director CTF Product Owner in Trial Management Systems will support ... wage for this position is $111,000 - $162,800 Purpose: Trial Management Systems as part of Clinical Trial...Technology and Process Implementation + System Owner for new capabilities which support drug development. + Drive the application… more
- Lilly (Indianapolis, IN)
- …solutions to support communities through philanthropy and volunteerism. **Purpose** : The Associate Director - Clinical Trial Foundations (CTF), will serve as ... collection systems, primarily focused on EDC and data aggregation systems. The Associate Director is responsible for collaborating with business partners to enable… more
- Lilly (Indianapolis, IN)
- …(CDDA) provides leadership in the strategy and development of contemporary clinical trial processes, technologies, information, and capabilities and in shaping ... should have extensive experience supporting data collection and aggregation systems. Clinical Trial Foundations as part of Clinical Design, Delivery & Analytics… more
- Lilly (Indianapolis, IN)
- …world's greatest health challenges. **Purpose:** This role is responsible for trial level clinical data strategy including database structure, content and meaning, ... and deliver clinical data management packages. This role is responsible for providing trial leadership and ownership for a particular trial , set of trials,… more
- Merck (Indianapolis, IN)
- **Job Description** **Job Description:** The Regional Medical Scientific Associate Director is a credentialed (ie, PhD, PharmD, DNP, MD) therapeutic and disease ... Scientific Congress Support, and Scientific Insights. Regional Medical Scientific Associate Director's liaise between the scientific community and the Company… more
- Merck (Indianapolis, IN)
- …with organizational priorities. Along with the USMA Field Leaders (Executive Director (ED)/ Associate Vice President (AV)), the SDMA is responsible for regional FM ... of Medical Affairs (RDMA) (where applicable), US Global Clinical Trial Organization, Global Medical and Scientific Affairs (GMSA) TA...therapeutic and competitive landscape to optimize US FM Team capabilities + May be responsible for one or more… more