MBBS Job – Manager Role at Lambda Therapeutic Research
If you are looking for a rewarding MBBS job in the clinical research field, this Manager position at Lambda Therapeutic Research offers an excellent career path. With growing interest in Lambda Therapeutic Research careers and opportunities across global research operations, this role gives MBBS professionals the chance to contribute to cutting-edge clinical studies while working with an internationally recognized CRO.
MBBS Job Details:
- Job Title: Manager
- Req ID: 1468
- Date: Nov 24, 2025
- Location: Ahmedabad, India
- Company: Lambda Therapeutic Research Ltd.
- CTC Range (INR): 800000 – 1500000
About the Company
Lambda Therapeutic Research Ltd. is a Global full-service Clinical Research Organization (CRO) with its headquarters in Ahmedabad, India. With facilities and operations strategically located in Mehsana (India), Las Vegas (USA), Toronto (Canada), Barcelona (Spain), London (UK), and Warsaw (Poland), we offer comprehensive end-to-end clinical research services to the global innovator, biotech, and generic pharmaceutical industries.
Qualifications
- M.B.B.S.
- 02–03 years of related experience
Job Description
This Manager role is an excellent MBBS job opportunity for professionals aiming to work in clinical research. The position involves functioning as a Co-Investigator / Study Physician, screening volunteers, conducting clinical examinations, reviewing protocols, managing safety issues, and ensuring compliance with SOPs and regulatory standards. It is a valuable step for candidates exploring Lambda Therapeutic Research careers and contributing to global studies through one of the most reputed Lambda Therapeutic Research jobs.
MBBS Job – Key Responsibilities:
- Act as a Co-Investigator / Study Physician
- Act as a screening physician- volunteers recruitment and screening
- Train and Guide Contractual staff for study-related activities and maintain training records
- Conduct clinical examinations and ascertain the eligibility of subjects for all clinical studies
- Coordinate with the screening and volunteer recruitment group on updates regarding volunteers adverse events and follow-up
- Prepare and review protocols for clinical studies
- Coordinate activities related to IEC & communicate issues to all concerned
- Ensure compliance with protocol, SOPs, and Regulatory requirements
- Coordinate with Project Coordinators for all project-related matters
- Monitor and manage adverse events, ensure timely response to QA findings
- Interact with sponsors on medical-related matters
- Handle safety-related issues and ensure appropriate communication
- Prepare and review reports for clinical studies
- Handle medical confidential reports and case management
- Help maintain and update all the systems and SOPs in the department
- Any other responsibilities as assigned by the Management / Head of the Department.
