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Manager – Clinical Research Operations

Lambda Research Accelerated
Lambda Research accelerated
2-3 years
INR 8 LPA – 15 LPA
Ahmedabad, India
1 May 8, 2026
Job Description
Job Type: Full Time Education: MBBS degree Skills: Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill

Manager – Clinical Research Operations
Location: Ahmedabad
Company: Lambda Therapeutic Research Ltd.
Job Type: Full-Time
Experience Required: 2–3 Years
Salary Range: INR 8 LPA – 15 LPA
Industry: Clinical Research / CRO / Pharmaceutical Research


About the Company

Lambda Therapeutic Research Ltd. is a globally recognized full-service Clinical Research Organization (CRO) headquartered in Ahmedabad, India. The organization provides end-to-end clinical research solutions to innovator, biotech, and generic pharmaceutical companies worldwide. With international operations across India, USA, Canada, Spain, UK, and Poland, Lambda Therapeutic Research delivers high-quality clinical development and research services aligned with global regulatory standards.


Job Overview

Lambda Therapeutic Research Ltd. is hiring experienced medical professionals for the position of Manager – Clinical Research Operations. The selected candidate will play a critical role in clinical trial management, volunteer screening, protocol compliance, adverse event monitoring, and coordination with sponsors and regulatory bodies.

This opportunity is ideal for MBBS professionals with hands-on experience in clinical research, study coordination, and subject management within a CRO or pharmaceutical environment.


Key Responsibilities

  • Act as a Co-Investigator and Study Physician for clinical studies
  • Conduct volunteer recruitment, screening, and clinical examinations
  • Assess subject eligibility for clinical trials as per protocol requirements
  • Coordinate with volunteer recruitment teams regarding adverse events and subject follow-ups
  • Prepare, review, and manage clinical study protocols and reports
  • Ensure compliance with SOPs, study protocols, regulatory guidelines, and ethical standards
  • Coordinate activities related to IEC submissions and communications
  • Work closely with Project Coordinators for study-related operations
  • Monitor adverse events and ensure timely resolution of QA observations
  • Interact with sponsors regarding medical and safety-related matters
  • Handle confidential medical reports and case management activities
  • Train and guide contractual staff involved in clinical study operations
  • Maintain and update departmental systems, documentation, and SOPs
  • Support additional responsibilities assigned by management or department heads

Required Qualifications

  • MBBS degree from a recognized institution
  • Strong understanding of clinical research processes and regulatory compliance
  • Knowledge of adverse event handling, protocol management, and subject safety procedures
  • Excellent communication, coordination, and documentation skills

Experience Requirements

  • Minimum 2 to 3 years of relevant experience in Clinical Research, CRO operations, or Study Management
  • Freshers are not eligible for this role

Preferred Skills

  • Clinical trial coordination
  • Volunteer screening and medical assessment
  • Regulatory and ethical compliance
  • Clinical documentation and reporting
  • Sponsor communication and project coordination
  • Team training and operational management

Why Join Lambda Therapeutic Research?

  • Opportunity to work with a globally established CRO
  • Exposure to international clinical research projects
  • Collaborative and research-driven work environment
  • Career growth opportunities in clinical operations and medical management
  • Competitive salary package and professional development support