Job Title: Research Associate – Volunteer Recruitment & Coordination
Req ID: 1306
Date: January 7, 2026
Location: Ahmedabad, India
Company: Lambda Therapeutic Research Ltd.
CTC Range (INR): 500,000 – 700,000
Lambda Therapeutic Research Ltd. is a global full-service Clinical Research Organization (CRO) headquartered in Ahmedabad, India. With strategically located facilities in Mehsana (India), Las Vegas (USA), Toronto (Canada), Barcelona (Spain), London (UK), and Warsaw (Poland), we provide comprehensive end-to-end clinical research services to global innovators, biotech companies, and pharmaceutical organizations.
Our mission is to deliver high-quality clinical research solutions with scientific integrity, regulatory compliance, and patient-focused excellence.
We are seeking an experienced Research Associate – Volunteer Recruitment & Coordination to manage volunteer recruitment, maintain the volunteer databank, and support clinical trial operations. The ideal candidate will have strong communication and organizational skills and experience in clinical volunteer management and study coordination.
Enhance and maintain the volunteer databank for clinical trials.
Conduct telecalling and field visits for volunteer recruitment and screening.
Ensure an adequate number of fit subjects are available and documented for ongoing trials.
Coordinate effectively between project coordinators and study volunteers.
Verify laboratory reports against requisitions to ensure accuracy.
Complete, compile, and review MSRs, consent for screening, and Participant Information Forms (PIFs).
Prepare volunteer ID cards and index cards for trial tracking.
Conduct post-study follow-ups with volunteers as required.
Participate in other project-related activities and support study teams as needed.
Perform additional responsibilities assigned by the Head of Department to meet project objectives.
5–7 years of experience in clinical research, volunteer recruitment, or study coordination.
Proven experience in volunteer management, clinical trial coordination, and field recruitment is preferred.
Any Graduate with strong communication and organizational skills.
Work in a global CRO with exposure to volunteer recruitment and clinical trial coordination.
Gain hands-on experience in clinical operations, data management, and subject handling.
Career growth opportunities through mentorship, training, and involvement in multiple therapeutic area studies.
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