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Manager - Scientific Management, Medical Services

1-2 years
₹14,00,000 – ₹18,00,000 per annum
10 Nov. 11, 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

Manager – Scientific Management, Medical Services

Company: Lambda Therapeutic Research Ltd.
Req ID: 1385
Location: Ahmedabad, India
Date Posted: 23 Oct 2025
CTC Range: ₹14,00,000 – ₹18,00,000 per annum


Company Overview

Lambda Therapeutic Research is a global full-service Clinical Research Organization (CRO) headquartered in Ahmedabad, India. With operations across:

  • Mehsana (India)

  • Las Vegas (USA)

  • Toronto (Canada)

  • Barcelona (Spain)

  • London (UK)

  • Warsaw (Poland)

Lambda provides end-to-end clinical research solutions to innovator, biotech, and generic pharmaceutical industries worldwide.


Job Summary

The Manager – Scientific Management (Medical Services) is responsible for feasibility assessment, medical writing, medical monitoring, and training activities for clinical trials. The role requires close collaboration with sponsors, investigators, and internal study teams to ensure scientific accuracy, regulatory compliance, and high-quality project execution.


Key Responsibilities

1. Feasibility Assessment

  • Prepare feasibility grids for clinical trials as per sponsor requirements.

  • Review Feasibility Questionnaires and feasibility reports.


2. Medical Writing

  • Prepare and review essential clinical documents, including:

    • Protocol synopsis

    • Study protocols

    • Investigator’s Brochure

    • Informed Consent Forms (ICFs)

    • Clinical Study Reports (CSRs)

    • Patient diaries, etc.

  • Coordinate with study teams, sponsors, and key opinion leaders (KOLs) to finalize all medical documents.


3. Medical Monitoring

On-site Monitoring Responsibilities:

  • Review Site Investigator Files, safety and SAE documentation, lab reports, X-ray/ECG reports, and other clinical data.

Remote Monitoring Responsibilities (Lambda Office):

  • Provide medical and technical guidance to investigators and study teams.

  • Offer clarifications on eligibility criteria, study procedures, participant continuation/discontinuation.

  • Review Adverse Events (AEs) and Serious Adverse Events (SAEs) to ensure accurate documentation and reporting.


4. Training

  • Train study teams on protocols, procedures, and study-related documents.

  • Provide departmental training on therapeutic and technical areas.

  • Participate in site initiation visits (SIVs).


5. General Responsibilities

  • Stay updated on clinical research advancements in India and globally.

  • Ensure compliance with all departmental quality systems, SOPs, and global regulatory guidelines.


Experience Required

  • 1–2 years of experience in Medical Monitoring within clinical research.


Educational Qualification

  • M.D. (Pharmacology)