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Senior Manager - Investigator & Physicians

Lambda Research Accelerated
Lambda Research accelerated
2-3 years
preferred by company
10 Dec. 24, 2025
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences 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

Req ID: 1313
Location: Ahmedabad, Gujarat, India
CTC Range: INR 12,00,000 – 18,00,000 per annum
Company: Lambda Therapeutic Research Ltd.
Industry: Clinical Research / CRO
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 Mehsana (India), Las Vegas (USA), Toronto (Canada), Barcelona (Spain), London (UK), and Warsaw (Poland), Lambda delivers end-to-end clinical research solutions to innovator, biotech, and generic pharmaceutical companies worldwide.

Position Overview

Lambda Therapeutic Research is seeking a qualified and experienced Senior Manager – Investigator & Physicians to support and lead medical and clinical oversight activities for clinical studies. The role involves investigator responsibilities, protocol feasibility assessments, regulatory compliance, safety oversight, and sponsor interaction across multiple clinical research programs.

Key Responsibilities

  • Conduct feasibility assessments of clinical study protocols and investigational molecules as requested by sponsors

  • Act as an Investigator, ensuring strict adherence to protocol inclusion/exclusion criteria and compliance requirements

  • Coordinate and supervise study teams to ensure compliance with protocols, SOPs, GCP, and applicable regulatory guidelines

  • Liaise with sponsors on medical and scientific matters related to ongoing and planned clinical studies

  • Communicate study updates, concerns, and safety issues with Institutional Ethics Committees (IEC) and local regulatory authorities

  • Monitor, manage, and oversee adverse events (AEs) and serious adverse events (SAEs) in coordination with study teams

  • Address safety-related issues and ensure appropriate documentation and timely reporting

  • Contribute to scientific and operational development initiatives within the organization

  • Maintain, review, and update departmental systems, SOPs, and clinical documentation

  • Support continuous improvement initiatives and compliance audits as required

Experience Required

  • Minimum 2–3 years of relevant experience in clinical research, preferably in investigator-led or physician oversight roles within a CRO or pharmaceutical organization

Educational Qualification

  • MD in Pharmacology (mandatory)

Why Join Lambda Therapeutic Research

  • Opportunity to work with a globally established CRO

  • Exposure to international clinical research projects

  • Collaborative and scientifically driven work environment

  • Competitive compensation aligned with industry standards

  • Career growth opportunities in clinical development and medical oversight

Lambda Therapeutic Research Ltd. is an equal opportunity employer and is committed to fostering a diverse, inclusive, and ethical workplace.