Medix™
Job Location :
Sacramento,CA, USA
Posted on :
2025-09-01T09:14:31Z
Job Description :
- Coordinate and conduct study visits as per protocol requirements.
- Screen, recruit, and enroll study participants; obtain informed consent.
- Collect and manage clinical data, including accurate entry into case report forms (CRFs) or electronic systems.
- Maintain study files and regulatory documentation in compliance with GCP and institutional guidelines.
- Schedule participant visits and follow-ups; ensure protocol adherence.
- Serve as a point of contact between study participants, investigators, and sponsors/monitors.
- Monitor and report adverse events in a timely manner.
- Assist with IRB submissions, amendments, and continuing reviews.
Apply Now!