Job Title: Senior Manager – Investigator & Physicians
Job Category: Clinical Research / Medical Affairs / Clinical Operations Leadership
Job Type: Full-Time
Location: Ahmedabad, Gujarat, India
Req ID: 1313
CTC Range: INR 12,00,000 – 18,00,000 per annum
Company Overview
Lambda Therapeutic Research Ltd. is a global full-service Clinical Research Organization (CRO) headquartered in Ahmedabad, India. The organization provides integrated, end-to-end clinical research services to innovator, biotechnology, and generic pharmaceutical companies worldwide.
With operations across India, North America, and Europe, Lambda supports global clinical development programs under stringent regulatory and ethical standards.
Role Overview
We are seeking a Senior Manager – Investigator & Physicians to lead medical oversight, investigator coordination, and regulatory compliance within clinical research programs. This role requires strong expertise in clinical trial feasibility, protocol review, safety monitoring, and stakeholder engagement with sponsors and regulatory bodies.
The ideal candidate will bring medical leadership experience and a deep understanding of GCP, ethical guidelines, and clinical study execution in regulated environments.
Key Responsibilities
Conduct feasibility assessments of investigational molecules as per sponsor requirements.
Review and evaluate clinical study protocols for scientific and regulatory alignment.
Ensure protocol adherence, eligibility criteria compliance, and regulatory standards during study execution.
Coordinate and supervise study teams to maintain compliance with SOPs, GCP guidelines, and applicable regulations.
Serve as a primary medical contact for sponsors regarding study-related medical queries and updates.
Liaise with Institutional Ethics Committees (IEC) and local regulatory authorities for study approvals and reporting.
Oversee safety management activities, including monitoring and reporting of Adverse Events (AE) and Serious Adverse Events (SAE).
Provide medical guidance to study teams for safety signal management and risk mitigation.
Contribute to the scientific and operational development of the department by updating SOPs, systems, and best practices.
Required Experience
2 to 3 years of relevant experience in clinical research, medical monitoring, or investigator roles within a CRO, hospital-based research unit, or pharmaceutical organization.
Demonstrated experience in protocol review, safety oversight, and regulatory compliance.
Strong knowledge of ICH-GCP guidelines, clinical trial regulations, and ethical frameworks.
Proven ability to interact with sponsors, investigators, and regulatory authorities.
Strong leadership, communication, and documentation skills.
Educational Qualification
MD in Pharmacology (mandatory).
Qualified medical professionals seeking leadership roles in clinical research and investigator management are encouraged to apply through ThePharmaDaily.com for confidential consideration.
Uttar Pradesh :
Agra | Gajraula | Gautam buddha Nagar | Ghaziabad | Gorakhpur | Greater Noida | Jhansi | kanpur | Lucknow | Mathura | Noida | Park City | Prayagraj | Satyamev | Varanasi |Gujarat :
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