Job Title: Senior Manager – Investigator & Physicians
Req ID: 1313
Date: January 14, 2026
Location: Ahmedabad, India
Company: Lambda Therapeutic Research Ltd.
CTC Range (INR): 1,200,000 – 1,800,000
Lambda Therapeutic Research Ltd. is a leading 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 end-to-end clinical research services to global innovators, biotech companies, and pharmaceutical organizations.
Our mission is to deliver high-quality clinical research and scientific solutions while maintaining regulatory compliance and advancing patient safety worldwide.
We are seeking an experienced Senior Manager – Investigator & Physicians to oversee clinical study feasibility, ensure protocol compliance, and provide scientific and medical leadership across clinical trials. The role requires close collaboration with sponsors, regulatory bodies, and internal study teams to ensure successful and compliant study execution.
Conduct feasibility assessments of investigational molecules and review clinical study protocols in response to sponsor requests.
Ensure adherence to protocol requirements during investigator assessments, including inclusion/exclusion criteria and compliance checks.
Coordinate and supervise the study team to ensure compliance with protocols, SOPs, and regulatory requirements throughout study conduct.
Serve as the primary point of contact for sponsors on medical and scientific matters, and liaise with Institutional Ethics Committees (IEC) and local regulatory authorities for study updates and concerns.
Monitor, manage, and report safety-related events, including adverse events (AEs) and serious adverse events (SAEs), in coordination with the study team.
Contribute to the scientific development of the organization by maintaining and updating departmental systems, SOPs, and knowledge resources.
Provide guidance to investigators and team members on clinical and regulatory best practices.
2–3 years of relevant experience in clinical research, investigator coordination, or physician-led study management.
Proven experience in protocol review, regulatory compliance, and clinical trial operations.
MD in Pharmacology or equivalent medical/scientific degree.
Opportunity to work in a global CRO with exposure to international clinical trials and regulatory standards.
Lead and mentor clinical teams while contributing to scientific and medical development.
Career growth with exposure to multiple therapeutic areas, investigator interactions, and global clinical operations.
Gujarat :
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