Medix™
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.