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Clinical Research Monitor-TIPS-3 PHRI Study

Clinical Research Monitor-TIPS-3 PHRI Study

ConfidentialBengaluru / Bangalore
24 days ago
Job description

Roles and Responsibilities :

Site Coordination

  • Assist senior team members in the coordination of ongoing clinical trials at assigned sites.

Training & Development

  • Undergo comprehensive training in monitoring processes and Good Clinical Practice (GCP).
  • Monitoring Activities

  • Schedule and conduct monitoring visits to clinical trial sites in accordance with the study protocol and regulatory requirements.
  • Site Support

  • Provide training to site personnel on GCP guidelines and specific study-related activities to ensure compliance.
  • Documentation & Reporting

  • Ensure accurate and timely documentation of monitoring visits and maintain detailed records in line with trial protocols.
  • Skills Required

    Site Monitoring, Documentation

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    Clinical Research • Bengaluru / Bangalore