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Senior Manager - Investigator & Physicians

Lambda Research Accelerated
Lambda Research accelerated
2-3 years
1200000 - 1800000
Ahmedabad, India
10 March 10, 2026
Job Description
Job Type: Full Time Education: MD 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

Job Title: Senior Manager – Investigator & Physicians

Company: Lambda Therapeutic Research Ltd.

Location: Ahmedabad, India

Req ID: 1313

Date Posted: Feb 12, 2026

Salary (CTC): ₹12,00,000 – ₹18,00,000 per year

Category: Clinical Research / Medical Leadership


Job Overview

The Senior Manager – Investigator & Physicians will lead and supervise clinical research activities while ensuring compliance with study protocols, regulatory requirements, and ethical guidelines. The role involves evaluating study feasibility, overseeing study teams, interacting with sponsors and regulatory bodies, and managing medical and safety aspects of clinical trials. The position also contributes to scientific development and continuous improvement of departmental systems and procedures.


Key Responsibilities

  • Conduct feasibility assessments of molecules based on sponsor requests and evaluate suitability for clinical studies.

  • Review clinical study protocols to ensure scientific validity and regulatory compliance.

  • Act as an Investigator and ensure all protocol requirements, eligibility criteria, and compliance checks are met.

  • Coordinate and supervise the Study Team to ensure adherence to study protocols, SOPs, and regulatory guidelines during trial execution.

  • Interact with study sponsors on medical and clinical matters related to ongoing studies.

  • Communicate with Institutional Ethics Committee (IEC) and local regulatory authorities regarding study updates and approvals.

  • Monitor and manage safety issues, including adverse events (AEs) and serious adverse events (SAEs).

  • Coordinate with the study team to ensure proper handling and reporting of safety events.

  • Contribute to the scientific development and strategic initiatives of the organization.

  • Maintain and update departmental systems, documentation, and SOPs.

  • Support quality standards and ensure continuous regulatory compliance in clinical operations.


Required Skills & Competencies

  • Strong understanding of clinical trial processes, medical monitoring, and regulatory requirements.

  • Knowledge of Good Clinical Practice (GCP), ethical guidelines, and regulatory frameworks.

  • Experience in protocol review, feasibility assessments, and clinical study oversight.

  • Ability to manage safety monitoring, adverse event reporting, and risk mitigation.

  • Strong leadership and team coordination skills.

  • Excellent communication skills for interaction with sponsors, investigators, and regulatory bodies.

  • Strong documentation and compliance management abilities.


Experience

  • 2–3 years of relevant experience in clinical research, preferably in investigator or physician roles within clinical research organizations (CROs), hospitals, or pharmaceutical companies.


Educational Qualification

  • MD in Pharmacology.