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Senior Manager - Investigator & Physicians

Lambda Therapeutic Research
Lambda Therapeutic Research
2-3 years
INR 12,00,000 – 18,00,000
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: Senior Manager – Investigator & Physicians

Req ID: 1313
Date Posted: September 20, 2025
Location: Ahmedabad, India
Company: Lambda Therapeutic Research Ltd.
CTC Range: INR 12,00,000 – 18,00,000


Educational Qualification

  • MD in Pharmacology


Experience

  • 2–3 years of relevant experience in clinical research or investigator management


Organisational Overview

  • Lambda Therapeutic Research is a global full-service Clinical Research Organization (CRO) headquartered in Ahmedabad, India, with facilities in Mehsana (India), Las Vegas (USA), Toronto (Canada), Barcelona (Spain), London (UK), and Warsaw (Poland).

  • The company provides end-to-end clinical trial services for biopharmaceutical and generic industries, emphasizing quality, innovation, and scientific expertise.


Job Overview

  • Lead and oversee clinical studies while ensuring compliance with protocols, SOPs, and regulatory requirements.

  • Serve as a key medical liaison between study teams, investigators, sponsors, and regulatory authorities.


Key Responsibilities

  • Conduct feasibility assessments of molecules based on sponsor requests.

  • Review clinical study protocols.

  • Act as an Investigator to ensure protocol compliance.

  • Coordinate and supervise the study team for adherence to SOPs, protocols, and regulatory standards.

  • Communicate with sponsors regarding medical matters.

  • Liaise with IEC and local regulatory authorities for study updates and concerns.

  • Handle and coordinate safety-related issues with the study team.

  • Monitor and manage adverse events (AEs) and serious adverse events (SAEs).

  • Contribute to scientific development and maintain departmental systems and SOPs.


Required Competencies

  • Strong knowledge of clinical study protocols and regulatory compliance.

  • Effective team coordination and investigator management skills.

  • Expertise in safety reporting and AE/SAE management.

  • Analytical thinking and problem-solving abilities.