Clinical Monitoring Jobs

Key Responsibilities:

• Verify that clinical trials are conducted in compliance with protocols, Good Clinical Practice (GCP), and regulatory requirements.
• Review site documents and ensure proper documentation of all study-related activities.
• Monitor patient safety by ensuring accurate and complete reporting of adverse events.

Key Responsibilities:

• Conduct site initiation, routine monitoring, and close-out visits.
• Train site staff on trial protocols and compliance requirements.
• Provide ongoing support and guidance to resolve site-related challenges.

Key Responsibilities:

• Verify data accuracy by cross-checking source documents with electronic data capture (EDC) systems.
• Identify discrepancies, raise queries, and collaborate with site staff to resolve them.
• Document all findings  in monitoring reports to maintain a clear audit trail.