Job Title: Manager – Clinical Research (Study Physician / Co-Investigator)
Req ID: 1468
Location: Ahmedabad, Gujarat, India
Company: Lambda Therapeutic Research Ltd.
CTC Range: INR 8,00,000 – 15,00,000 per annum
Experience Required: 2–3 years of relevant clinical research experience
Job Type: Full-Time | On-Site | Permanent
Job Category: Clinical Research | Medical Affairs | Drug Safety | CRO Operations
About the Company
Lambda Therapeutic Research Ltd. is a global full-service Clinical Research Organization (CRO) headquartered in Ahmedabad, India. With operational facilities in Mehsana (India), Las Vegas (USA), Toronto (Canada), Barcelona (Spain), London (UK), and Warsaw (Poland), the organization delivers comprehensive end-to-end clinical research services to global innovators, biotechnology companies, and generic pharmaceutical organizations.
The company specializes in Phase I–IV clinical trials, regulatory compliance, medical oversight, pharmacovigilance, and global study execution.
Role Overview
The Manager – Clinical Research will function as a Study Physician and Co-Investigator, supporting the medical conduct of clinical trials while ensuring subject safety, regulatory compliance, and protocol adherence. The role involves volunteer recruitment oversight, clinical evaluations, adverse event management, and sponsor interaction within a regulated CRO environment.
This position is ideal for MBBS professionals seeking to advance their career in clinical trials, pharmacovigilance, and medical monitoring.
Key Responsibilities
Act as Co-Investigator and Study Physician for assigned clinical studies
Serve as Screening Physician for volunteer recruitment and eligibility assessment
Conduct detailed clinical examinations and confirm subject eligibility
Train and guide contractual staff for study-related activities and maintain training documentation
Coordinate with screening and recruitment teams regarding adverse events and subject follow-up
Prepare and review clinical study protocols and related documentation
Manage Institutional Ethics Committee (IEC) submissions and communications
Ensure compliance with approved protocols, SOPs, ICH-GCP guidelines, and regulatory requirements
Collaborate with Project Coordinators for seamless study execution
Monitor, assess, and manage adverse events and safety-related issues
Ensure timely and appropriate responses to Quality Assurance (QA) findings
Interact with sponsors on medical and safety matters
Prepare, review, and maintain clinical study reports and confidential medical case documentation
Support the maintenance and continuous improvement of departmental systems and SOPs
Perform additional responsibilities as assigned by management or department leadership
Required Experience
2–3 years of experience in clinical research, clinical trials, or hospital-based clinical practice
Exposure to ICH-GCP guidelines and regulatory compliance preferred
Experience in volunteer screening, adverse event monitoring, and clinical documentation is advantageous
Strong understanding of medical case management and safety reporting processes
Effective communication skills for sponsor and cross-functional coordination
Educational Qualifications
MBBS (Bachelor of Medicine and Bachelor of Surgery) – Mandatory
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