This job posting has expired
Expired on April 1, 2026
Clinical Trials E-Source Implementation Specialist
Job Description
Responsible for creating, configuring, and optimizing electronic source templates across clinical trials. Ensure source document templates accurately reflect protocol and compliant study conduct.
Responsibilities
- Create and configure electronic source templates
- Optimize e-source templates across clinical trials
- Ensure templates reflect protocol requirements
- Support efficient and compliant study conduct
Qualifications
- Bachelor's degree or equivalent
- Previous experience as a Clinical Research Coordinator (CRC)
- Experience building E-Source in CRIO
- Knowledge of Good Clinical Practice (GCP) guidelines