Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Senior Manager - Investigator & Physicians

Lambda Therapeutic Research
Lambda Therapeutic Research
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.