Sun Pharma Laboratories Ltd is hiring for the position of Clinical Research Associate (CRA) in its Medical Affairs & Clinical Research business unit. The opportunity is based in Delhi and is open to candidates with a Bachelor’s or Master’s degree in a health-related field and 1–5 years of relevant clinical research experience.
The selected candidate will be responsible for clinical trial site management, investigator coordination, regulatory submissions, site monitoring, patient recruitment, safety reporting, and coordination with CRO partners.
Sun Pharma Clinical Research Associate – Job Details
| Particulars | Details |
|---|---|
| Company | Sun Pharma Laboratories Ltd |
| Job Role | Clinical Research Associate |
| Business Unit | Medical Affairs & Clinical Research |
| Location | Delhi |
| Experience | 1–5 Years |
| Qualification | Bachelor’s / Master’s Degree in a Health-Related Field |
| Job Posted Date | 12 November 2026 |
Positions
- Clinical Research Associate (CRA)
Job Responsibilities
The Clinical Research Associate will handle the following responsibilities:
- Conduct site feasibility assessments, identify potential investigators, negotiate study budgets, and finalize investigators and clinical trial sites.
- Execute Confidentiality Disclosure Agreements (CDAs) and study-related contracts.
- Prepare and submit study documents to Ethics Committees (ECs) for approval across respective study centres.
- Oversee investigational product (IP) dispensing, inventory management, and reconciliation.
- Coordinate site initiation, site monitoring, and site close-out activities, ensuring timely completion of monitoring reports.
- Train investigators and site personnel on study protocols, procedures, and Good Clinical Practice (GCP) principles.
- Ensure timely recruitment of clinical trial participants.
- Monitor data entry, source data verification (SDV), and clinical data query resolution.
- Ensure timely reporting of Serious Adverse Events (SAEs) and Suspected Unexpected Serious Adverse Reactions (SUSARs), including communication to sites and investigators in accordance with regulations and Sun Pharma pharmacovigilance policies.
- Identify and assess site-related risks and implement Corrective and Preventive Actions (CAPA) for sites not meeting expectations.
- Coordinate with internal teams and CRO partners for data management, statistical analysis, statistical analysis reports, and database lock (DBL).
Eligibility and Educational Qualifications
Candidates must meet the following educational and experience requirements:
Educational Qualification:
- Bachelor’s degree in a health-related field such as Biology, Chemistry, Nursing, Pharmacy, or Public Health.
- Master’s degree in a relevant health-related field.
- Postgraduate Diploma in Clinical Research.
Experience:
- 1–5 years of relevant experience in Clinical Research.
Required Skills and Knowledge
Based on the listed job responsibilities, the role involves working knowledge of:
- Clinical trial site management and monitoring.
- Site feasibility and investigator coordination.
- Clinical trial documentation and Ethics Committee submissions.
- Good Clinical Practice (GCP) principles.
- Investigational Product (IP) management.
- Patient recruitment and source data verification.
- SAE and SUSAR reporting.
- Risk assessment and CAPA management.
- Clinical data management and CRO coordination.
