Looking for Site Management Operations Jobs in Ahmedabad? Lambda Therapeutic Research is hiring professionals with an MD in Pharmacology/Clinical Pharmacology for its Site Management Operations team. This opportunity is ideal for candidates with 0-3 years of experience who want to build a career in Clinical Research, Clinical Operations, Medical Monitoring, Pharmacovigilance, and Oncology Clinical Research.
The selected candidates will support clinical trial operations, provide medical and scientific expertise, collaborate with investigators, and ensure compliance with ICH-GCP and regulatory guidelines. If you’re searching for Clinical Research Jobs in India 2026, this is an excellent opportunity to join one of India’s leading Contract Research Organizations (CROs).
Job Details
| Particular | Details |
|---|---|
| Company | Lambda Therapeutic Research |
| Job Role | Site Management Operations |
| Location | Ahmedabad, Gujarat |
| Experience | 0โ3 Years |
| Qualification | MD Pharmacology / MD Clinical Pharmacology |
| Employment Type | Full-Time, Permanent |
| Industry | Clinical Research / Contract Research |
| Department | Healthcare & Life Sciences |
| Salary | โน16โ20 LPA (Approx.) |
| Openings | 2 |
Key Responsibilities
As a Site Management Operations professional at Lambda Therapeutic Research, you will:
Site Management Operations
- Support site identification and feasibility assessments.
- Coordinate site initiation, maintenance, and close-out activities.
- Act as the primary contact for investigators and research sites.
- Manage regulatory documents and study records.
- Monitor site performance and protocol compliance.
- Resolve operational and protocol-related issues.
Medical & Scientific Oversight
- Provide medical and pharmacology expertise to investigators.
- Review clinical protocols and informed consent documents.
- Assess patient eligibility.
- Interpret inclusion and exclusion criteria.
- Review laboratory data, medical history, and safety information.
Clinical Trial Management
- Support Phase IโIV clinical studies.
- Monitor study timelines and recruitment goals.
- Ensure compliance with ICH-GCP, NDCTR, CDSCO, and SOPs.
- Participate in monitoring visits and quality improvement initiatives.
- Assist during audits and regulatory inspections.
Oncology Clinical Research Support
- Provide expertise in oncology studies.
- Support patient screening and recruitment.
- Guide investigators on oncology endpoints and treatment protocols.
Pharmacovigilance & Safety
- Review Adverse Events (AEs) and Serious Adverse Events (SAEs).
- Support safety reporting activities.
- Assist with causality assessment.
- Collaborate with Pharmacovigilance and Medical Monitoring teams.
Regulatory Compliance
- Support Ethics Committee submissions.
- Maintain Trial Master File (TMF) documentation.
- Ensure compliance with regulatory guidelines.
Educational Qualification
Candidates should possess:
- MD in Pharmacology
- OR MD in Clinical Pharmacology
Experience Required
- 0โ3 years
- Experience in any of the following is preferred:
- Site Management Operations
- Clinical Research
- Clinical Operations
- Medical Monitoring
- Pharmacovigilance
- Oncology Clinical Research
Preferred Skills
- Clinical Trial Management
- ICH-GCP Guidelines
- CDSCO Regulations
- NDCTR Compliance
- Site Management
- Oncology Research
- Pharmacovigilance
- Medical Monitoring
- Regulatory Documentation
- Clinical Protocol Review
- TMF Management
- Safety Data Review
- Investigator Coordination
Why Join Lambda Therapeutic Research?
- Opportunity to work with a leading Clinical Research Organization.
- Exposure to global clinical trials.
- Hands-on experience in oncology research.
- Career growth in Clinical Operations and Site Management.
- Competitive salary package.
- Collaborative work environment.
- Opportunities to work alongside experienced medical professionals.
How to Apply
