Manager – Clinical Research
Lambda Therapeutic Research Ltd. | Ahmedabad, India
Req ID: 1468
Posted On: 24 November 2025
Experience Required: 2–3 years
Education: MBBS
Salary (CTC): INR 8,00,000 – 15,00,000 per annum
Location: Ahmedabad, India
About the Organization
Lambda Therapeutic Research Ltd. is a global full-service Clinical Research Organization (CRO) headquartered in Ahmedabad, India. With operations across India, USA, Canada, Spain, UK, and Poland, Lambda delivers end-to-end clinical development solutions to innovator, biotech, and generic pharmaceutical companies worldwide.
The organization is recognized for its scientific expertise, regulatory compliance, and large-scale clinical research capabilities. Lambda’s multi-geography network enables the delivery of high-quality clinical outcomes with speed, precision, and operational excellence.
Role Overview
Lambda Therapeutic Research is seeking a qualified Manager – Clinical Research (MBBS) to support medical oversight and clinical operations across studies. This role involves medical review, subject safety management, protocol development, and coordination with cross-functional teams. The ideal candidate will have strong clinical judgment, experience in study conduct, and the ability to interact with regulatory bodies and sponsors.
Key Responsibilities
Serve as Co-Investigator / Study Physician for assigned clinical studies.
Perform volunteer recruitment, screening, and medical examinations to determine subject eligibility.
Train and guide contractual staff on study-specific procedures and maintain training documentation.
Coordinate with screening and volunteer management teams for updates on adverse events and follow-up.
Prepare, review, and provide medical input for clinical study protocols.
Manage IEC submissions, communications, and regulatory compliance activities.
Ensure adherence to protocols, SOPs, GCP guidelines, and applicable regulatory requirements.
Collaborate with Project Coordinators and cross-functional teams to ensure smooth study execution.
Monitor, document, and manage adverse events; ensure timely resolution of QA observations.
Interact with sponsors and stakeholders regarding medical aspects of ongoing studies.
Handle safety issues, confidential medical data, and clinical case management.
Prepare and review clinical study reports and medical summaries.
Support continuous improvement of departmental systems and SOPs.
Perform additional tasks as assigned by senior management or the department head.
Experience Required
2 to 3 years of relevant experience in clinical research, clinical practice, or study physician roles.
Educational Qualifications
MBBS from a recognized institution.
Gujarat :
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