Lambda Careers: Apply Now for a Manager Position
Lambda Careers: Lambda Therapeutic Research Ltd. is seeking a qualified manager (study physician) to strengthen its clinical research operations in Ahmedabad. This role is ideal for medical professionals looking to transition or advance within the clinical research and CRO domain, offering direct involvement in clinical studies, subject safety oversight, and collaboration with global sponsors. The position provides an opportunity to work in a regulated, science-driven environment that supports professional growth and global exposure.
Lambda Careers: Job Details
- Job Title: Manager
- Req ID: 1468
- Location: Ahmedabad, India
- Employment Type: Full-time
- CTC Range: ₹800,000 – ₹1,500,000 per annum
About the Company
Lambda Therapeutic Research is a global, full-service Clinical Research Organization (CRO) headquartered in Ahmedabad, India. The organization delivers end-to-end clinical research services to innovator, biotechnology, and generic pharmaceutical companies worldwide.
With operational presence across India (Ahmedabad & Mehsana), the USA (Las Vegas), Canada (Toronto), the UK (London), Spain (Barcelona), and Poland (Warsaw), Lambda combines scientific rigor, regulatory excellence, and operational scalability. The company is recognized for its expertise in early-phase to late-phase clinical trials, bioavailability/bioequivalence studies, and global regulatory compliance.
Lambda Careers: Qualifications
- Educational Qualification: MBBS (Mandatory)
- Experience: 2–3 years of relevant clinical or clinical research experience
- Strong understanding of clinical research protocols, SOPs, and regulatory guidelines
- Strong communication, documentation, and coordination skills
About the Role
The manager role functions as a study physician/co-investigator, playing a critical role in the execution of clinical studies. The position involves medical oversight of clinical trials, volunteer screening, safety monitoring, and close collaboration with internal teams, ethics committees, and sponsors. The role ensures that all clinical activities are conducted ethically, safely, and in compliance with regulatory standards.
Key Responsibilities
- Act as co-investigator/study physician for assigned clinical studies
- Conduct clinical examinations and determine subject eligibility
- Oversee volunteer recruitment, screening, and follow-up for adverse events
- Ensure compliance with study protocols, SOPs, and regulatory requirements
- Coordinate with IEC, project coordinators, QA teams, and sponsors
- Monitor and manage adverse events and safety-related issues
- Prepare, review, and maintain clinical study documentation and reports
- Maintain medical confidentiality and case management standards
- Support the continuous improvement of departmental systems and SOPs
Why Join Lambda Therapeutic Research?
- Opportunity to work with a globally recognized CRO
- Exposure to international clinical research projects
- Strong focus on regulatory compliance and scientific excellence
- Competitive compensation aligned with industry standards
- Professional growth in medical affairs and clinical research leadership
- Collaborative, structured, and research-driven work culture
