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Manager - Investigator & Physicians

3+ years
INR 8,00,000 – 10,00,000
10 Oct. 7, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/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

Job Title: Manager – Investigator & Physicians

Req ID: 1386
Date Posted: October 3, 2025
Location: Mehsana, India
Company: Lambda Therapeutic Research Ltd.
CTC Range: INR 8,00,000 – 10,00,000


Organizational Overview

Lambda Therapeutic Research Ltd. is a leading global Clinical Research Organization (CRO) headquartered in Ahmedabad, India, with operations in Mehsana (India), Warsaw (Poland), London (UK), Pittsburgh (USA), Las Vegas (USA), and Fargo (USA). The company has over 1500 employees worldwide.

Key Highlights:

  • Over 20 years of service in clinical research

  • Provides full-spectrum clinical trial solutions for biopharmaceutical and generic industries

  • Focus on quality, innovation, and therapeutic expertise for safe and effective product development

  • Committed to hiring qualified and energetic professionals with a desire for excellence


Job Overview

The Manager – Investigator & Physicians will function as a Principal Investigator / Co-Investigator and coordinate clinical research activities, ensuring compliance with protocols, regulatory standards, and SOPs.


Key Responsibilities

  • Function as a Principal Investigator / Co-Investigator for clinical studies

  • Prepare and review protocols for clinical trials

  • Coordinate activities related to Institutional Ethics Committee (IEC)

  • Communicate IEC-related issues to all concerned parties

  • Ensure compliance with study protocols, SOPs, and regulatory requirements

  • Coordinate with Project Coordinators on all project-related matters

  • Monitor and manage adverse events during clinical trials

  • Consult with panel of medical experts as required

  • Ensure timely response to QA findings

  • Interact with sponsors regarding medical matters

  • Handle safety-related issues and ensure proper communication

  • Prepare and review clinical study reports


Required Experience

  • Minimum 3 years of experience in clinical research or related field


Educational Qualification

  • Doctorate in a related discipline


Skills & Competencies

  • Strong knowledge of clinical research protocols and regulatory requirements

  • Ability to coordinate with multiple stakeholders, including IEC and sponsors

  • Effective communication and reporting skills

  • Expertise in adverse event monitoring and management