- 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 ... with key study partners to define, implement, and deliver clinical data management packages. This role is... trial leadership and ownership for a particular trial , set of trials , or programs. **Primary… more
- Lilly (Indianapolis, IN)
- …dissemination, and preparation of final reports and publications. + Take part in the reporting of clinical trial data in Clinical Trial Registry ... activities over the entire spectrum of drug development and clinical trial phases. Specific activities include developing...of responsibility, the development, conduct and reporting of local clinical trials ; the implementation of global … more
- Lilly (Indianapolis, IN)
- …of external health care professionals according to guidelines above. + Participate in reporting of clinical trial data in Clinical Trial Registry ... participates in: the development, conduct and reporting of corporate/global clinical trials in support of registration and...clinical data relevant to the molecule. Clinical Research/ Trial Execution and Support + Plans,… more
- Lilly (Indianapolis, IN)
- …The Clinical Study Build Programmer is responsible for programming and testing clinical trial data collection databases, including the mapping, testing ... and associated data repository mappings for a trial or set of trials within a...a deep understanding of the technology used to collect clinical trial data + Effectively… more
- Lilly (Indianapolis, IN)
- … Study Build Programmer - eCOA** is responsible for programming and testing clinical trial data collection databases, including the mapping, testing ... and associated data repository mappings for a trial or set of trials within a...a deep understanding of the technology used to collect clinical trial data + Develops… more
- Lilly (Indianapolis, IN)
- … dissemination, and preparation of final reports and publications. + Participate in reporting of clinical trial data in Clinical Trial Registry ... activities over the entire spectrum of drug development and clinical trial phases. Specific activities include developing...area of responsibility, the development, conduct and reporting of clinical trials ; the implementation of global … more
- Sumitomo Pharma (Indianapolis, IN)
- …with cross-functional teams to ensure proper execution and conduct of the clinical trial ; generates quality clinical data . + Serves as primary contact ... timelines. + Monitors the status of clinical data collection of assigned clinical trials...clinical trials and basic knowledge of clinical trial outcome standards. + Strong analytical… more
- Lilly (Indianapolis, IN)
- …of external health care professionals according to guidelines above. + Participate in reporting of clinical trial data in Clinical Trial Registry ... clinical practices. She/He will conduct and support clinical trials in each phase of development....LRL priorities. + Understand and keep updated with the pre- clinical and clinical data relevant… more
- Sumitomo Pharma (Indianapolis, IN)
- …conduct of clinical trials and handling administrative aspects of clinical trial execution. This role will support completion of all study deliverables, ... highly motivated, and experienced individual for the position of ** Clinical Trial Associate (CTA)** **.** The ...ensuring the highest level of data quality; proactively identifies, communicates, and resolves … more
- Sumitomo Pharma (Indianapolis, IN)
- …seeking a dynamic, highly motivated, and experienced individual for the position of ** Clinical Trial Associate for Study Start-up** **.** The Clinical ... requirements. + Perform general administrative tasks to support team members with clinical trial execution, eg, development and formatting of documents, review… more