Desun Hospital is hiring a Clinical Research Associate (CRA) in Kolkata for professionals with 1–2 years of clinical trial monitoring experience. This CRA job in Kolkata offers hands-on exposure to site monitoring, ICH-GCP compliance, TMF management, and regulatory documentation within a hospital-based clinical research environment.
If you are looking to grow your career in clinical research associate jobs in India, this opportunity provides structured monitoring responsibilities, direct investigator coordination, and regulatory compliance oversight.
Author: Pharmabharat Editorial Team
Industry: Clinical Research / Contract Research
Employment Type: Full-Time, Permanent
Location: Kolkata, West Bengal
Key Responsibilities – Clinical Research Associate (CRA)
The selected Clinical Research Associate will be responsible for:
- Conducting Site Selection Visits (SSV), Site Initiation Visits (SIV), Interim Monitoring Visits (IMV), and Close-Out Visits (COV)
- Ensuring trials comply with ICH-GCP guidelines, SOPs, and regulatory requirements
- Monitoring study progress for adherence to protocol, timelines, and quality benchmarks
- Performing Source Data Verification (SDV) and validating CRF/eCRF entries
- Identifying and documenting protocol deviations and discrepancies
- Maintaining and updating the Trial Master File (TMF)
- Ensuring informed consent process compliance
- Coordinating with investigators, site staff, CROs, and sponsors
- Tracking and reporting Serious Adverse Events (SAEs)
- Preparing detailed monitoring reports and follow-up letters
- Supporting audit and inspection readiness
This Clinical Research Associate job in Kolkata requires strong documentation skills and a deep understanding of regulatory compliance frameworks.
Eligibility & Qualifications
Educational Qualification:
- B.Pharm / M.Pharm / BSc / MSc (Life Sciences, Pharmacy, Clinical Research, or related field)
Experience:
- 1–2 years of experience in clinical trial monitoring
- Working knowledge of ICH-GCP guidelines
- Experience in TMF maintenance and SAE reporting
Required Skills:
- Clinical trial monitoring
- Source data verification (SDV)
- eCRF documentation
- Regulatory compliance knowledge
- Strong communication & coordination skills
Why Apply for This CRA Job in Kolkata?
- Exposure to real-time hospital-based clinical trials
- Experience in end-to-end monitoring lifecycle
- Strong foundation in regulatory documentation
- Career growth in Clinical Research Associate domain
- Opportunity to work with multidisciplinary healthcare teams
This role is ideal for candidates aiming to build a long-term career in Clinical Research Associate (CRA) roles in India.
How to Apply?
