Posted:3 months ago|
Platform:
On-site
Full Time
Assist in site selection, initiation, monitoring, and close-out visits.
Ensure that clinical trials are conducted in accordance with protocols, SOPs, GCP, and regulatory requirements.
Verify the accuracy and completeness of case report forms (CRFs) and source documents.
Maintain essential documents in the Trial Master File (TMF).
Assist in resolving data queries and discrepancies with the site staff.
Support investigators and site staff in trial-related activities.
Participate in project team meetings and training sessions.
Prepare visit reports and follow-up letters.
Maintain regular communication with study sites to ensure compliance and timely data entry.
CLARIWELLGLOBAL SERVICES LLP
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