- Elevance Health (Indianapolis, IN)
- **Nurse and CPC - Clinical Fraud Investigator II - SIU Fraud & Abuse** **Location:** This position will work a hybrid model (remote and office). The ideal ... Workplace Strategy:** 1-2 days in office per week The **Clinical Fraud Investigator II ** is responsible for identifying issues and/or entities that may pose… more
- TEKsystems (Indianapolis, IN)
- …ideas and unique point of view, consider working at Labcorp as an Investigator Support Coordinator. The Investigator Support Coordinator is responsible for the ... fax. In more details, you will be * Notifying investigator sites, sponsors, and affiliates of laboratory results, sponsor...liaison for both internal and external clients * Communicating investigator site needs when new policies or procedures are… more
- Merck (Indianapolis, IN)
- …interest to the company. The RMSD provides research support to our Investigator -Sponsored and Company-Sponsored Trials to enhance the understanding of the scientific ... patient enrollment and retention efforts for a given study or address Investigator questions. RMSDs also respond to scientific questions from SLs, including… more
- Lilly (Indianapolis, IN)
- …the clinical program and trial design of assets approaching and/or primarily in Phases II to IV. In order to accomplish this, the **Clinical Design Physician** must ... of the **Clinical Design Physician** are focused on the design of Phase II to Phase IV clinical programs and studies within the therapeutic area. The… more
- Lilly (Indianapolis, IN)
- …clinical program and trial design of assets approaching and/or primarily in Phases II to IV (including Real World Evidence generation). In order to accomplish this, ... Design Physician are focused on the design of Phase II to Phase IV clinical programs and studies within...of study/protocol design features to feasibility, value, patient and investigator burden, and execution speed/efficiency. + Contribute to the… more
- Lilly (Indianapolis, IN)
- …compounds, but can also include early phase trials (for example, phase I and II trials). The CRP is responsible for collaborating with the global teams in the ... of phase 3b /4 studies (and phase I and II studies where applicable), as well as non clinical...of protocols and data collection requirements. ▪ Participate in investigator identification and selection, in conjunction with clinical teams.… more
- Merck (Indianapolis, IN)
- …and goals for approved, in-development, and active Company-sponsored trials and/or investigator -sponsored research studies. The RMSD serves as a role model for ... Enhances the comprehension of the scientific foundations and goals of investigator -sponsored research + Identifies barriers to patient enrollment and retention… more
- Merck (Indianapolis, IN)
- …for approved, in-development, and active Company-sponsored trials and/or investigator -sponsored research studies. The Regional Medical Scientific Director serves ... Enhances the comprehension of the scientific foundations and goals of investigator -sponsored research + Identifies barriers to patient enrollment and retention… more
- Merck (Indianapolis, IN)
- …for approved, in-development, and active company-sponsored trials and/or investigator -sponsored research studies. The Regional Medical Scientific Director serves ... Enhances the comprehension of the scientific foundations and goals of investigator -sponsored research. + Identifies barriers to patient enrollment and retention… more
- Merck (Indianapolis, IN)
- …and goals for approved, in-development, and active Company-sponsored trials and/or investigator -sponsored research studies. The RMSD serves as a role model for ... approved, in development and active Company-Sponsored Trials and/or company Investigator -Sponsored Program (MISP) and Oncology Translational Studies Program (OTSP)… more
- Merck (Indianapolis, IN)
- …and goals for approved, in-development, and active Company-sponsored trials and/or investigator -sponsored research studies and serve as a role model for other ... Enhances the comprehension of the scientific foundations and goals of investigator -sponsored research. + Identifies barriers to patient enrollment and retention… more
- Lilly (Indianapolis, IN)
- …but can also include early phase trials (for example, phase I and II trials). The Senior/Executive Director is responsible for the planning, startup and conduct ... development of protocols and data collection requirements. + Participate in investigator identification and selection, in conjunction with clinical teams. + Ensure… more