Sun Pharmaceutical Industries Ltd. is inviting applications for the position of Clinical Research Associate (CRA) in Mumbai, Maharashtra. This opportunity is suitable for candidates with a background in pharmacy, life sciences, healthcare, nursing, or clinical research who have relevant experience in clinical trial management and site monitoring.
The selected candidate will work in the Clinical Research business unit and support clinical studies by coordinating with investigators, managing study documentation, monitoring trial sites, and ensuring compliance with Good Clinical Practice (GCP) and applicable regulatory requirements.
Candidates with 2–5 years of relevant clinical research experience and knowledge of Phase III and Phase IV clinical trials can review the eligibility criteria and job responsibilities below.
Sun Pharma Clinical Research Associate Recruitment 2026: Job Highlights
| Particulars | Details |
|---|---|
| Company | Sun Pharma |
| Job Title | Clinical Research Associate |
| Department | Clinical Research |
| Job Location | Mumbai, Maharashtra |
| Office Location | Sun House – Corporate Office |
| Experience Required | 2–5 years |
| Qualification | Bachelor’s or Master’s degree in a relevant field and/or postgraduate diploma in Clinical Research |
| Industry | Pharmaceutical / Clinical Research |
| Employment Type | Not specified in the available job description |
| Salary | Not disclosed |
| Job Posting Date | October 24, 2026 |
| Application Mode | Online through the company’s careers portal |
About Sun Pharma
Sun Pharma is a pharmaceutical company focused on developing and delivering medicines across multiple therapeutic areas. The company promotes continuous learning, collaboration, professional development, and employee growth.
This Clinical Research Associate position offers an opportunity to contribute to clinical research activities while coordinating with investigators, clinical trial sites, internal teams, and contract research organisation (CRO) partners.
Job Description: Clinical Research Associate
The Clinical Research Associate will be responsible for supporting clinical trials from site feasibility and initiation through monitoring and close-out. The role involves investigator coordination, regulatory documentation, investigational product management, participant recruitment oversight, clinical data quality, and safety reporting.
The candidate will also collaborate with cross-functional teams and external partners to help ensure that clinical studies progress according to the study protocol, regulatory requirements, and company procedures.
Key Responsibilities
1. Clinical Trial Site Management
- Conduct site feasibility assessments and identify suitable investigators and clinical trial sites.
- Coordinate investigator selection and negotiate study budgets with potential investigators.
- Facilitate the finalisation of investigators and sites, including the execution of confidentiality disclosure agreements (CDAs) and study-related contracts.
- Ensure timely site initiation, routine monitoring, and site close-out activities.
- Prepare and maintain the required site monitoring reports.
2. Regulatory and Ethics Committee Documentation
- Prepare and submit study documents to the Ethics Committee (EC) for approval or permission across participating centres.
- Ensure that study documentation is appropriately maintained in line with applicable regulatory guidelines and company procedures.
- Support compliance with Good Clinical Practice (GCP) principles and clinical trial requirements.
3. Investigational Product Management
- Oversee and document investigational product (IP) dispensing at clinical trial sites.
- Maintain inventory records and ensure proper reconciliation of investigational products.
- Monitor product accountability and documentation throughout the study.
4. Investigator Training and Site Coordination
- Train investigators and site personnel on the study protocol, clinical trial procedures, and GCP principles.
- Coordinate with investigators and site teams to address operational challenges.
- Support effective communication between trial sites and internal clinical research teams.
5. Patient Recruitment and Clinical Data Quality
- Monitor participant recruitment against the clinical study plan.
- Ensure timely and accurate clinical data entry.
- Perform source data verification (SDV) to check clinical trial data against source records.
- Follow up on data queries and support their timely resolution.
6. Clinical Trial Safety Reporting
- Ensure timely reporting of serious adverse events (SAEs) and suspected unexpected serious adverse reactions (SUSARs), as applicable.
- Coordinate required SAE communications with sites and investigators.
- Follow applicable regulatory requirements and Sun Pharma pharmacovigilance policies.
7. Risk Management and CAPA
- Identify and assess risks at clinical trial sites.
- Analyse site performance issues and coordinate corrective and preventive actions (CAPA) where required.
- Follow up on sites that are not meeting study expectations or planned timelines.
8. Coordination with CRO and Internal Teams
- Coordinate with in-house teams and contract research organisation (CRO) partners.
- Support data management and statistical analysis activities.
- Coordinate deliverables related to statistical analysis reports and database lock (DBL).
Eligibility Criteria
Educational Qualification
Applicants should have a Bachelor’s or Master’s degree in a health-related or relevant discipline, such as:
- Biology
- Chemistry
- Nursing
- Pharmacy
- Public Health
A postgraduate diploma in Clinical Research is also mentioned in the job requirements. Candidates should review the employer’s application criteria to confirm the qualification pathway applicable to them.
Work Experience
Candidates should have 2–5 years of relevant experience in clinical research.
Experience related to clinical trial site management, investigator coordination, site monitoring, regulatory documentation, and clinical study operations may be relevant to the responsibilities of this position.
Required Skills
Applicants should possess the following knowledge and capabilities:
- Good Clinical Practice (GCP) and clinical trial regulatory guidelines.
- Knowledge of Phase III and Phase IV clinical trials.
- Clinical trial site management and monitoring.
- Investigator and clinical site coordination.
- Clinical study documentation and regulatory submissions.
- Clinical data entry, source data verification, and query resolution.
- Clinical trial safety reporting requirements.
- Risk assessment and corrective and preventive action (CAPA).
- Collaboration with cross-functional teams and CRO partners.
Job Location
The position is based in Mumbai, Maharashtra, at Sun House – Corporate Office.
Candidates should review the official vacancy details for any additional information regarding working arrangements, reporting structure, travel requirements, or other employment conditions.
Salary and Benefits
The salary for the Clinical Research Associate position has not been specified in the available job description.
Sun Pharma highlights employee well-being, professional development, collaboration, and opportunities for growth. However, specific benefits, compensation details, and other employment terms should be confirmed directly with the company during the recruitment process.
How to Apply for Sun Pharma Recruitment 2026
Interested and eligible candidates can check the official Sun Pharma careers website for the Clinical Research Associate vacancy in Mumbai.
Application steps:
- Visit the official Sun Pharma website.
- Navigate to the Careers section.
- Search for “Clinical Research Associate” and select Mumbai as the location.
- Open the matching vacancy and review the complete job requirements.
- Submit your application through the official application process, if the vacancy is available.
Before applying, confirm that the job title and location match the vacancy you are interested in. The link above leads to the company’s careers section and is not a direct application link for this specific position.
Frequently Asked Questions (FAQs)
1. What is the job role announced by Sun Pharma?
Sun Pharma has listed a vacancy for a Clinical Research Associate in its Clinical Research business unit.
2. Where is the Clinical Research Associate job located?
The position is based in Mumbai, Maharashtra, at Sun House – Corporate Office.
3. How much experience is required for this position?
The stated experience requirement is 2–5 years in the field of clinical research.
4. What qualifications are required for Sun Pharma CRA recruitment?
The job description mentions a Bachelor’s or Master’s degree in a relevant health-related field, such as Biology, Chemistry, Nursing, Pharmacy, or Public Health, and/or a postgraduate diploma in Clinical Research.
5. Is experience in clinical trials required?
Yes. Relevant clinical research experience is required. Knowledge of Phase III and Phase IV clinical trials is specifically mentioned.
6. What skills are important for this job?
Key skills include GCP knowledge, regulatory compliance, clinical trial site management, investigator coordination, and collaboration with cross-functional stakeholders.
7. What are the main responsibilities of a Clinical Research Associate?
The role includes site feasibility, investigator selection, site initiation and monitoring, regulatory documentation, investigational product accountability, participant recruitment oversight, data verification, safety reporting, and coordination with CRO partners.
8. What is the salary for the Sun Pharma Clinical Research Associate position?
The salary has not been disclosed in the available vacancy details. Candidates can enquire about compensation during the recruitment process.
9. How can I apply for this vacancy?
Visit the official Sun Pharma Careers website and search for the Clinical Research Associate position in Mumbai. Follow the instructions provided on the relevant vacancy page.
10. What is the application deadline?
The available job description is dated October 24, 2026, but it does not specify an application deadline. Check the official careers portal for the current status of the vacancy.
Disclaimer
This article has been prepared for informational purposes based on the supplied job description. Vacancy availability, eligibility requirements, responsibilities, and employment conditions may change. The application deadline, salary, and specific benefits were not provided in the supplied details. Candidates should verify the latest information on the official Sun Pharma careers website before applying.