Clinical Trials Administrator - India

About the role

The Clinical Trials Administrator [CTA] is responsible for coordinating clinical trial activities from study set-up through closeout, ensuring accurate documentation, data quality, regulatory compliance, and timely project deliverables.

What you'll do

• Review Clinical Trial Protocols and assist with protocol set-up functions as required
• Develops the Protocol Test Summary (PTS), Global Laboratory Specification Document (GLSD), Investigator Laboratory Manual and protocol specific operating procedures
• Support day to day project related activities once the study is live
• Coordination with Sponsor, CRO & Alliance laboratory for each project
• Participate in study conference calls with clients

What you need

• 1–2 yrs of experience
• Clinical research
• Quality control
• CRO
• Test cases
• Phlebotomy
• SOP writing
• Any graduate

Good to have

• Microbiology
• Chemistry
• GCP