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Manager - Scientific Management, Medical Services

2-3 years
12,00,000 – 18,00,000 per annum
5 Dec. 2, 2025
Job Description
Job Type: Full Time Education: MBBS, MD Pharmacology 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

Lambda Therapeutic Research | Ahmedabad, India

Req ID: 1385
Posted On: 21 November 2025
Experience Required: 1–2 years (Medical Monitoring)
Salary (CTC): ₹14,00,000 – ₹18,00,000 per annum
Location: Ahmedabad, India
Company: Lambda Therapeutic Research Ltd.


About Lambda Therapeutic Research

Lambda Therapeutic Research Ltd. is a global full-service Clinical Research Organization (CRO) headquartered in Ahmedabad, India. The organization supports end-to-end clinical research needs for innovator, biotech, and generic pharmaceutical companies.
Lambda operates across multiple international locations, including Mehsana (India), Las Vegas (USA), Toronto (Canada), Barcelona (Spain), London (UK), and Warsaw (Poland). With extensive expertise in clinical development, medical affairs, and regulatory operations, Lambda is recognized for its scientific excellence and global capability footprint.


Role Overview

The Manager – Scientific Management, Medical Services will support clinical trial feasibility, medical writing, and medical monitoring activities. The role requires strong scientific judgment, therapeutic area knowledge, and the ability to collaborate with cross-functional clinical teams and external stakeholders. This position is ideal for candidates with 1–2 years of experience in medical monitoring who wish to advance their career in clinical development within a global CRO.


Key Responsibilities

1. Feasibility Grid Preparation

  • Conduct feasibility assessments for clinical trials based on sponsor requirements.

  • Review feasibility questionnaires and prepare detailed feasibility reports to support study planning.

2. Medical Writing

  • Prepare and review essential study documents, including:

    • Protocol Synopses

    • Study Protocols

    • Investigator’s Brochures

    • Informed Consent Forms

    • Clinical Study Reports

    • Patient Diaries and related materials

  • Coordinate with study teams, sponsors, and key opinion leaders to finalize study-related documents with scientific accuracy.

3. Medical Monitoring

At Site Level:

  • Review Site Investigator Files, safety documentation, SAE reports, laboratory data, X-ray and ECG reports.

Remote Monitoring (Lambda Office):

  • Provide guidance to investigators and study teams on eligibility criteria, study procedures, and patient continuation/discontinuation decisions.

  • Review adverse events and Suspected/Serious Adverse Events (SAEs) to ensure complete, accurate, and timely documentation and reporting.

4. Training Responsibilities

  • Train study teams on study protocols and trial-specific documentation.

  • Deliver departmental training sessions on therapeutic areas and technical concepts.

  • Participate in site initiation visits as required.

5. General Responsibilities

  • Stay updated on advancements in clinical research, regulations, and therapeutic developments.

  • Ensure adherence to departmental quality standards and process improvement initiatives.

  • Maintain scientific, operational, and regulatory compliance across assigned responsibilities.


Experience Required

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


Educational Qualification

  • M.D. in Pharmacology is mandatory.