- Lilly (Indianapolis, IN)
- …to support communities through philanthropy and volunteerism. Purpose: The purpose of the Associate - Clinical Trial Foundations (CTF) Business role is ... the Clinical Design, Delivery and Analytics (CDDA) organization. The Associate - Clinical Trial Foundations (CTF) Business is responsible and/or assists… more
- Sumitomo Pharma (Indianapolis, IN)
- …are currently seeking a dynamic, highly motivated, and experienced individual for the position of ** Clinical Trial Associate (CTA)** **.** The Clinical ... conduct of clinical trials and handling administrative aspects of clinical trial execution. This role will support completion of all study deliverables,… more
- Lilly (Indianapolis, IN)
- …who are determined to make life better for people around the world. Purpose: The Associate Director, Clinical Trial Foundations (CTF), will serve as the ... subject matter expert for clinical systems supporting clinical development. In this...and assisting the team to prepare for inspections. The Associate Director is responsible for collaborating with business partners… more
- Sumitomo Pharma (Indianapolis, IN)
- …currently seeking a dynamic, highly motivated, and experienced individual for the position of ** Clinical Trial Associate for Study Start-up** **.** The ... Clinical Trial Associate for Study Start-up (SSU CTA) assists in the delivery of site start up activities for assigned studies from site identification… more
- Lilly (Indianapolis, IN)
- …proofs. + Review/approve allowable dating, stability justifications and retest dating for clinical trial (CT) Materials. + Provide Quality oversight for ... (QA) is responsible for providing quality oversight of all materials used in clinical trials. PRD QA CT Packaging is responsible for oversight of packaging and… more
- Lilly (Indianapolis, IN)
- …position 3 days onsite/2 days remote **Purpose:** This role is responsible for trial level clinical data strategy including database structure, content and ... with key study partners to define, implement, and deliver clinical data management packages. This role is responsible for...data management packages. This role is responsible for providing trial leadership and ownership for a particular trial… more
- Lilly (Indianapolis, IN)
- … Study Build Programmer - eCOA** is responsible for programming and testing clinical trial data collection databases, including the mapping, testing and ... collaborate with Data and Analytics colleagues such as the Clinical Data Associate , Clinical Data...a deep understanding of the technology used to collect clinical trial data + Develops and tests… more
- Lilly (Indianapolis, IN)
- … Clinical Study Build Programmer is responsible for programming and testing clinical trial data collection databases, including the mapping, testing and ... collaborate with Data and Analytics colleagues such as the Clinical Data Associate , Clinical Data...a deep understanding of the technology used to collect clinical trial data + Effectively apply knowledge… more
- IQVIA (Indianapolis, IN)
- …to join our team. In this role, you will be responsible for monitoring clinical trial sites to ensure compliance with study protocols, regulatory guidelines, and ... IQVIA Biotech is hiring for our Early Clinical Development team. Ideal candidates will have Phase...site documentation is properly maintained and filed in the Trial Master File (TMF) and Investigator Site File (ISF)… more
- Lilly (Indianapolis, IN)
- …of disease prevalence, etc.), analyses and insights to drive excellence in clinical trial design, enabling more efficient planning and execution to ... people around the world. **Purpose:** The purpose of the Associate Director Analysis role is to support the design...Apply novel techniques to add efficiency and automation into Clinical Trial Design and CDDA capabilities +… more