Sun Pharma Laboratories Ltd is hiring for the position of Clinical Research Associate (CRA) in Mumbai, Maharashtra. The role is part of the Clinical Research business unit and involves clinical trial site management, investigator coordination, regulatory documentation, patient recruitment monitoring, and compliance with Good Clinical Practice (GCP) guidelines.
Candidates with a bachelor’s or master’s degree in a relevant health or science field and 2β5 years of clinical research experience can review the eligibility requirements below.
Job Details
| Particulars | Details |
|---|---|
| Company | Sun Pharma Laboratories Ltd |
| Job Role | Clinical Research Associate |
| Business Unit | Clinical Research |
| Job Location | Mumbai, Maharashtra |
| Experience | 2β5 years |
| Qualification | Bachelor’s or Master’s degree in a relevant field and/or Postgraduate Diploma in Clinical Research |
| Job Posting Date | October 24, 2026 |
Positions
The job description lists the position of Clinical Research Associate within Sun Pharma’s Clinical Research business unit in Mumbai.
Key Responsibilities
The selected candidate will be responsible for the following activities:
- Conduct site feasibility assessments and identify potential investigators.
- Negotiate study budgets and finalize investigators and clinical trial sites.
- Coordinate the execution of Confidentiality Disclosure Agreements (CDAs) and study-related contracts.
- Prepare and submit study documents for Ethics Committee (EC) approval across study centres.
- Oversee investigational product (IP) dispensing, inventory management, and reconciliation.
- Ensure timely site initiation, monitoring, and close-out activities, including the preparation of monitoring reports.
- Train investigators and site personnel on study protocols, procedures, and GCP principles.
- Monitor participant recruitment, data entry, source data verification, and query resolution.
- Ensure timely reporting of Serious Adverse Events (SAEs) and Suspected Unexpected Serious Adverse Reactions (SUSARs), in accordance with applicable regulations and Sun Pharma pharmacovigilance policies.
- Identify site-related risks, conduct risk analysis, and implement Corrective and Preventive Actions (CAPA).
- Coordinate with internal teams and Contract Research Organization (CRO) partners on data management, statistical analysis, statistical analysis reports, and database lock (DBL).
Eligibility and Qualifications
Candidates should meet the educational and experience requirements outlined in the job description.
Educational qualifications:
- Bachelor’s or Master’s degree in a health-related or relevant scientific field, such as Biology, Chemistry, Nursing, Pharmacy, or Public Health.
- A Postgraduate Diploma in Clinical Research is also listed as a relevant qualification.
Experience:
- 2β5 years of relevant experience in clinical research.
Required Skills
Applicants should have the following knowledge and competencies:
- Understanding of Good Clinical Practice (GCP) and clinical trial regulatory guidelines.
- Knowledge and expertise in Phase III and Phase IV clinical trials.
- Clinical trial site management expertise.
- Ability to collaborate with cross-functional stakeholders.
