Clinical Research Associate

Job Summary

We are looking for detail-oriented and motivated Clinical Research Associates (CRAs) to support clinical trials and ensure compliance with Good Clinical Practice (GCP), applicable regulatory requirements, and clinical study protocols.

Key Responsibilities

• Monitor clinical trial sites to ensure compliance with study protocols and GCP guidelines.
• Assist in site selection, initiation, monitoring, and close-out visits.
• Verify clinical trial data for accuracy, completeness, and consistency.
• Maintain Trial Master Files (TMF) and essential study documentation.
• Coordinate with investigators, site staff, sponsors, and clinical research teams.
• Identify protocol deviations and support their resolution.
• Ensure participant safety, confidentiality, and proper informed consent documentation.
• Prepare monitoring visit reports and follow up on outstanding action items.
• Support regulatory documentation and clinical trial reporting activities.