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Clinical Trial Manager

2-3 years
8-12 LPA
10 Dec. 2, 2025
Job Description
Job Type: Full Time Education: MBBS Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

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.