Manager – Clinical Research (Study Physician)
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
Employment Type: Full-time
About the Organization
Lambda Therapeutic Research Ltd. is a globally recognized, full-service Clinical Research Organization (CRO) headquartered in Ahmedabad, India. With a strong international presence across India, the USA, Canada, Spain, the UK, and Poland, Lambda delivers comprehensive end-to-end clinical research services to innovator, biotech, and generic pharmaceutical companies worldwide. The organization is known for its regulatory excellence, scientific integrity, and patient-centric clinical development approach.
Job Overview
Lambda Therapeutic Research is seeking a qualified and experienced Manager (Clinical Research / Study Physician) to support and manage clinical trial activities. This role is ideal for an MBBS-qualified professional with hands-on experience in clinical research, subject safety management, and regulatory compliance. The position plays a critical role in ensuring ethical, medical, and regulatory standards across clinical studies.
Key Responsibilities
Act as Co-Investigator / Study Physician for assigned clinical trials
Perform duties as a Screening Physician, including volunteer recruitment and medical screening
Conduct comprehensive clinical examinations and determine subject eligibility
Train and guide contractual staff on study-related activities and maintain training records
Coordinate with volunteer recruitment teams regarding adverse events and subject follow-ups
Prepare, review, and support clinical study protocols and medical reports
Liaise with Independent Ethics Committees (IEC) and communicate study-related updates
Ensure strict compliance with study protocols, SOPs, ICH-GCP, and regulatory guidelines
Coordinate with Project Coordinators for study execution and timelines
Monitor, assess, and manage adverse events (AEs) and respond to QA findings
Act as a medical point of contact for sponsors on safety and clinical matters
Handle safety reporting, medical case management, and confidential documentation
Support the maintenance and continuous improvement of departmental SOPs and systems
Perform additional responsibilities as assigned by the Head of Department or Management
Required Experience
2 to 3 years of relevant experience in clinical research, clinical trials, or a healthcare research environment
Experience in subject screening, safety monitoring, and protocol compliance is preferred
Educational Qualification
MBBS from a recognized medical institution
Key Skills & Competencies
Strong knowledge of clinical trial conduct and regulatory requirements
Understanding of GCP, SOPs, and ethical guidelines
Excellent clinical judgment and documentation skills
Effective communication and coordination with cross-functional teams
Ability to manage safety issues and medical reporting independently
Why Join Lambda Therapeutic Research
Work with a globally reputed CRO on diverse clinical projects
Gain exposure to international clinical research standards
Collaborative and professional work environment
Strong opportunities for career growth in clinical research and medical leadership
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