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Manager - Scientific Management, Medical Services

1-2 years
INR 14,00,000 – 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: Manager – Scientific Management, Medical Services

Req ID: 1385
Date Posted: September 24, 2025
Location: Ahmedabad, India
Company: Lambda Therapeutic Research Ltd.
CTC Range: INR 14,00,000 – 18,00,000


Organizational 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).

Key Highlights:

  • Provides comprehensive end-to-end clinical research services to global innovator, biotech, and generic pharmaceutical industries


Department: Medical Services

Designation: Manager – Scientific Management
Education Required: M.D. in Pharmacology
Experience Required: 1–2 years in Medical Monitoring


Job Overview

The Manager will oversee medical monitoring, feasibility assessment, and medical writing for clinical trials, ensuring compliance, quality, and alignment with sponsor requirements.


Key Responsibilities

Feasibility Grid Preparation

  • Prepare feasibility for clinical trials as per sponsor requirements

  • Review feasibility questionnaires and feasibility reports

Medical Writing

  • Prepare and review study-related documents (Protocol Synopsis, Study Protocols, Investigator’s Brochure, Informed Consent Forms, Clinical Study Reports, Patient Diaries, etc.)

  • Liaise with study teams, sponsors, and key opinion leaders to finalize study documents

Medical Monitoring

  • At site level: Review Site Investigator File, Safety and SAE reporting documents, Laboratory documents, X-ray and ECG reports

  • At office level: Provide guidance to PIs/study teams on eligibility criteria, study procedures, patient continuation/discontinuation

  • Review adverse events and SAEs and ensure proper recording and reporting

Training

  • Train study team members on study protocols and related documents

  • Train department members on therapeutic and technical areas

  • Conduct site initiation visits

General Duties

  • Stay updated on developments in clinical research in India and globally

  • Comply with departmental quality initiatives


Required Competencies

  • Clinical knowledge and medical monitoring expertise

  • Strong medical writing and documentation skills

  • Ability to train and guide study teams

  • Awareness of regulatory compliance and quality standards