MBBS Job at Lambda Therapeutic Research in Ahmedabad | Apply
If you are looking for a rewarding MBBS Job in the clinical research industry, this opportunity at Lambda Therapeutic Research Ltd. could be the perfect next step in your medical career. This MBBS Job in Ahmedabad offers hands-on involvement in clinical studies, regulatory coordination, and medical management within a global Clinical Research Organization. Explore one of the leading lambda therapeutic research jobs and advance your professional journey in clinical research.
Job Details
- Job Title: Manager
- Req ID: 1468
- Date: Feb 19, 2026
- Location: Ahmedabad, India
- Company: Lambda Therapeutic Research Ltd.
- CTC Range (INR): 800000 – 1500000
About the Company
Lambda Therapeutic Research 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. As part of growing lambda therapeutic research jobs, this organization provides strong career opportunities for medical professionals seeking an advanced MBBS Job in the clinical research sector.
Job Description
This MBBS Job in Ahmedabad involves working as a Co-Investigator / Study Physician within a reputed CRO environment. The role includes screening volunteers, conducting clinical examinations, ensuring regulatory compliance, and coordinating with multiple departments for the smooth execution of clinical studies.
Professionals applying for this MBBS Job will be responsible for medical oversight, safety monitoring, sponsor interaction, and maintaining adherence to SOPs and regulatory requirements.
- Educational Qualification: M.B.B.S.
- Experience: 02-03 years of related experience
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 and 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.
