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Senior Manager - Investigator & Physicians

2-3 years
12,00,000 – 18,00,000 per annum
10 Dec. 2, 2025
Job Description
Job Type: Full Time Education: MBBS, MD Pharmacology 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

Senior Manager – Investigator & Physicians

Lambda Therapeutic Research Ltd. | Ahmedabad, India

Req ID: 1313
Posted On: 17 November 2025
Experience Required: 2–3 years
Educational Qualification: MD – Pharmacology
Salary (CTC): INR 12,00,000 – 18,00,000 per annum
Location: Ahmedabad, India


Company Overview

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 comprehensive end-to-end clinical research solutions to innovator pharma, biotech, and generic drug industries.

With decades of scientific leadership, Lambda specializes in bioequivalence, pharmacokinetics, pharmacodynamics, early-phase and late-phase clinical trials, regulatory strategy, clinical operations, and global project management. The organization is recognized for its high-quality research, world-class infrastructure, and strong medical and scientific expertise.


Role Overview

The Senior Manager – Investigator & Physicians will support clinical study execution, protocol adherence, safety oversight, and sponsor communication. This role serves as a scientific and operational bridge between investigators, study teams, regulatory bodies, and sponsors.


Key Responsibilities

Protocol & Feasibility

  • Conduct feasibility assessments of new molecules based on sponsor requirements.

  • Review clinical study protocols and ensure medical and operational feasibility.

Clinical Oversight & Compliance

  • Serve as the Investigator responsible for ensuring full compliance with protocol requirements during eligibility assessments and study conduct.

  • Supervise and guide the study team to maintain adherence to SOPs, GCP guidelines, and regulatory expectations.

Sponsor & Regulatory Communication

  • Liaise with sponsors on all medical and clinical matters.

  • Communicate study updates to the Institutional Ethics Committee (IEC) and local regulatory authorities.

Safety Management

  • Oversee safety-related activities, including real-time monitoring of AEs and SAEs.

  • Coordinate with the study team to ensure timely assessment, documentation, and management of safety events.

Scientific & Organizational Contribution

  • Support the scientific growth of the department through inputs on process enhancements and best practices.

  • Contribute to the development, review, and updating of departmental systems and SOPs.


Required Experience

  • 2–3 years of relevant experience in clinical research, pharmacology, or investigator-led operations within CROs or clinical trial sites.


Required Qualification

  • MD – Pharmacology from a recognized medical institution.