Perform site initiation, routine monitoring, and close-out visits.
Review and verify case report forms (CRFs) against source documents.
Identify and resolve data discrepancies.
Ensure proper documentation and timely reporting of adverse events.
Maintain effective communication with investigators, sponsors, and regulatory authorities.
Assist in the preparation of regulatory submissions and documentation.
Provide training and support to site staff as needed.
Help ensure that sites comply with protocols, GCP guidelines, and regulatory requirements.
Support the initiation, monitoring, and close-out of clinical trial sites under supervision.
Employement Category:
Employement Type: Full timeIndustry: Medical / HealthcareRole Category: Allied Health ServicesFunctional Area: Not SpecifiedRole/Responsibilies: Clinical Research Associate