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Manager

Lambda Therapeutic Research
Lambda Therapeutic Research
2-3 years
800000 - 1500000
Ahmedabad, India
10 April 22, 2026
Job Description
Job Type: Full Time Education: M.B.B.S. 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

Organisational Overview

Company Name: Lambda Therapeutic Research

Lambda Therapeutic Research is a global, full-service Clinical Research Organization (CRO) headquartered in Ahmedabad, India. The organization has strategically located facilities and operations in:

  • Mehsana (India)
  • Las Vegas (USA)
  • Toronto (Canada)
  • Barcelona (Spain)
  • London (UK)
  • Warsaw (Poland)

Core Capabilities

Lambda provides comprehensive end-to-end clinical research services to:

  • Innovator pharmaceutical companies
  • Biotechnology firms
  • Generic pharmaceutical industries

Job Details / Key Responsibilities

1. Clinical Role

  • Act as:
    • Co-Investigator / Study Physician
    • Screening Physician for volunteer recruitment
  • Perform:
    • Clinical examinations
    • Subject eligibility assessment for clinical studies

2. Volunteer Management

  • Oversee:
    • Volunteer recruitment and screening
  • Coordinate with recruitment teams regarding:
    • Adverse events
    • Follow-ups

3. Training & Supervision

  • Train and guide contractual staff for study-related activities
  • Maintain training records

4. Protocol & Documentation

  • Prepare and review:
    • Clinical study protocols
    • Study reports

5. Regulatory & Ethical Compliance

  • Coordinate activities related to:
    • IEC (Institutional Ethics Committee)
  • Ensure compliance with:
    • Study protocols
    • SOPs
    • Regulatory requirements

6. Study Coordination

  • Coordinate with:
    • Project Coordinators for study-related matters
  • Communicate important updates/issues to all stakeholders

7. Safety & Adverse Event Management

  • Monitor and manage:
    • Adverse events
    • Safety-related issues
  • Ensure:
    • Timely response to QA findings
    • Proper communication of safety concerns

8. Sponsor & Stakeholder Interaction

  • Interact with sponsors on:
    • Medical-related matters

9. Data Handling & Confidentiality

  • Manage:
    • Medical confidential reports
    • Case management processes

10. System & SOP Maintenance

  • Maintain and update:
    • Departmental systems
    • Standard Operating Procedures (SOPs)

11. Additional Responsibilities

  • Perform any other tasks assigned by:
    • Management
    • Head of Department