Sun Pharma Hiring Clinical Research Associate (CRA) in Mumbai & Delhi | Apply for Clinical Research Jobs
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Sun Pharma Hiring Clinical Research Associate (CRA) |
Introduction
Clinical Research continues to be one of the most promising career domains for Pharmacy, Life Sciences, Nursing, and Healthcare professionals. With increasing investments in drug development, clinical trials, regulatory research, and patient safety programs, pharmaceutical companies are actively hiring skilled Clinical Research Associates (CRAs) to support clinical trial operations and ensure regulatory compliance.
Sun Pharma Laboratories Ltd has announced recruitment for the position of Clinical Research Associate (CRA) under its Medical Affairs & Clinical Research division. This opportunity is ideal for professionals with 1–5 years of experience in clinical trial monitoring, investigator management, site coordination, ethics committee submissions, and GCP compliance.
Candidates looking to build a long-term career in Clinical Operations, Clinical Trial Management, Pharmacovigilance Coordination, and Medical Affairs can benefit significantly from this opportunity with one of India's largest pharmaceutical companies.
About Sun Pharma
Sun Pharmaceutical Industries Limited is one of the largest specialty generic pharmaceutical companies in the world. The company manufactures and markets a broad range of pharmaceutical formulations and active pharmaceutical ingredients across multiple therapeutic segments.
With operations spanning more than 100 countries, Sun Pharma has built a strong reputation for innovation, quality, regulatory compliance, and global healthcare solutions. The company invests heavily in research, development, clinical studies, and medical affairs activities to support product development and patient care worldwide.
Company Overview
Company Name: Sun Pharmaceutical Industries Limited
Founded: 1983
Founder: Dilip Shanghvi
Headquarters: Mumbai, Maharashtra, India
Global Presence: 100+ Countries
Employees: Approximately 38,000+ worldwide
Industry: Pharmaceuticals & Healthcare
Sun Pharma continues to be one of the most sought-after employers for professionals pursuing careers in Clinical Research, Pharmacovigilance, Regulatory Affairs, Quality Assurance, and Medical Affairs.
Job Overview Summary
The Clinical Research Associate (CRA) position is responsible for supporting and monitoring clinical trial activities at investigator sites while ensuring compliance with protocol requirements, Good Clinical Practice (GCP), ethical standards, and regulatory guidelines.
The selected candidate will work closely with investigators, ethics committees, CROs, site staff, data management teams, and internal stakeholders to ensure smooth execution of clinical studies.
This role provides hands-on exposure to site monitoring, source data verification, clinical operations, patient recruitment management, SAE reporting, and investigator relationship management.
Vacancy Details
| Particular | Details |
|---|
| Position | Clinical Research Associate (CRA) |
| Company | Sun Pharma Laboratories Ltd |
| Department | Medical Affairs & Clinical Research |
| Job Type | Full-Time |
| Location | Mumbai & Delhi |
| Experience | 1–5 Years |
| Industry | Clinical Research |
| Employment Type | Permanent |
Job Role Explanation
What Does a Clinical Research Associate Do?
A Clinical Research Associate serves as the bridge between sponsors, investigators, CROs, and study sites during clinical trial execution.
The CRA ensures that clinical studies are conducted according to:
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Study Protocols
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Good Clinical Practice (GCP)
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ICH Guidelines
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Regulatory Requirements
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Ethics Committee Requirements
Clinical Research Associates play a critical role in maintaining trial quality, participant safety, data integrity, and regulatory compliance throughout the study lifecycle.
This position is considered one of the most important roles in Clinical Operations and often serves as a gateway to higher-level clinical research positions.
Key Responsibilities
The selected Clinical Research Associate may perform the following responsibilities:
Site Feasibility Assessment
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Evaluate potential clinical trial sites
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Assess investigator suitability
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Support site selection activities
Investigator & Site Management
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Coordinate with investigators and study teams
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Maintain investigator relationships
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Support site performance improvement
Budget & Contract Activities
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Participate in site budget discussions
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Support contract execution
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Manage Confidentiality Disclosure Agreements (CDAs)
Ethics Committee Submissions
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Prepare submission documents
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Coordinate ethics committee approvals
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Maintain regulatory documentation
Clinical Trial Monitoring
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Conduct Site Initiation Visits (SIV)
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Perform Monitoring Visits (MV)
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Conduct Close-Out Visits (COV)
Source Data Verification (SDV)
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Verify clinical trial data accuracy
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Resolve data discrepancies
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Support database quality
Investigational Product Management
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Monitor IP inventory
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Reconcile investigational products
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Ensure accountability compliance
Safety Reporting Activities
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Support SAE reporting
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Assist SUSAR reporting processes
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Coordinate with Pharmacovigilance teams
Risk & CAPA Management
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Identify site-related risks
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Implement Corrective and Preventive Actions (CAPA)
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Monitor study performance
Eligibility Criteria
Applicants should possess any of the following qualifications:
Educational Qualification
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B.Pharm
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M.Pharm
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B.Sc Life Sciences
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M.Sc Life Sciences
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Nursing Degree
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Bachelor's Degree in Biology
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Bachelor's Degree in Chemistry
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Public Health Degree
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Post Graduate Diploma in Clinical Research
Experience Requirement
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1–5 years of Clinical Research experience
Preferred Experience
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Clinical Trial Monitoring
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Site Management
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Investigator Coordination
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Ethics Committee Submission
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GCP Compliance
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Clinical Trial Operations
Skills Required
Successful candidates should demonstrate expertise in:
Clinical Research Skills
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Clinical Trial Monitoring
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Site Management
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Clinical Operations
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Trial Documentation
Regulatory Knowledge
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ICH Guidelines
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Good Clinical Practice (GCP)
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Ethics Committee Requirements
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Regulatory Compliance
Technical Competencies
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Source Data Verification (SDV)
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SAE Reporting
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SUSAR Reporting
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CAPA Management
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Database Coordination
Professional Skills
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Communication Skills
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Documentation Skills
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Problem Solving
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Project Coordination
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Stakeholder Management
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Time Management
Salary Estimate
Sun Pharma has not officially disclosed the compensation package for this role.
Based on similar Clinical Research Associate positions in India, the estimated salary range may be:
Estimated Salary
₹5.5 LPA – ₹11 LPA
Compensation may vary based on:
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Clinical Research Experience
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Monitoring Exposure
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Clinical Trial Expertise
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Interview Performance
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Internal Salary Structure
Additional benefits may include:
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Medical Insurance
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Learning Programs
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Career Development Opportunities
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Performance Incentives
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Clinical Research Certifications Support
Interview Details
The official interview schedule has not been announced.
The selection process may include:
Round 1
Application Screening
Round 2
HR Evaluation
Round 3
Clinical Research Technical Interview
Round 4
Hiring Manager Discussion
Round 5
Final Selection & Offer
Candidates should prepare for questions related to:
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GCP Guidelines
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ICH Requirements
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Site Monitoring
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SDV
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SAE Reporting
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Ethics Committee Processes
Required Documents
Applicants should keep the following documents ready:
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Updated Resume
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Educational Certificates
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Degree Certificates
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Clinical Research Training Certificates
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Experience Certificates
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Current Salary Documents
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Government ID Proof
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Passport-size Photograph
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Relieving Letter (if applicable)
How to Apply
Interested candidates can apply through the official Sun Pharma career portal.
Apply through the Mumbai Clinical Research Associate vacancy.
Apply through the Delhi Clinical Research Associate vacancy.
Candidates should ensure that their resume highlights:
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Clinical Trial Monitoring Experience
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Site Management Activities
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GCP Knowledge
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Ethics Committee Submission Experience
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Clinical Operations Exposure
Why Join Sun Pharma?
Working at Sun Pharma offers exposure to:
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Multicenter Clinical Trials
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Global Clinical Research Standards
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Medical Affairs Operations
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Investigator Management
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Clinical Development Programs
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Regulatory Compliance Systems
Professionals can build strong long-term careers in:
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Clinical Operations
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Clinical Trial Management
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Medical Affairs
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Pharmacovigilance
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Regulatory Affairs
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Project Management
Frequently Asked Questions (FAQs)
1. Who can apply for this Clinical Research Associate role?
Candidates with qualifications in Pharmacy, Life Sciences, Nursing, Biology, Chemistry, Public Health, or Clinical Research can apply.
2. What experience is required?
Applicants should have 1–5 years of relevant Clinical Research experience.
3. What are the job locations?
The openings are available in Mumbai and Delhi.
4. Is monitoring experience preferred?
Yes. Site monitoring, SDV, and investigator management experience are highly preferred.
5. What are the major responsibilities of a CRA?
Clinical trial monitoring, site management, ethics submissions, GCP compliance, SDV, and safety reporting.
6. Is GCP knowledge mandatory?
Yes. Good Clinical Practice (GCP) understanding is one of the core requirements.
7. What career growth opportunities are available?
Professionals can advance toward Senior CRA, Clinical Trial Manager, Clinical Project Manager, Medical Affairs Specialist, and Clinical Operations Manager roles.
Final Conclusion
The Sun Pharma Clinical Research Associate (CRA) vacancy provides an excellent opportunity for Clinical Research professionals seeking career advancement in one of India's leading pharmaceutical organizations. With exposure to clinical trial monitoring, investigator management, GCP compliance, ethics committee submissions, and safety reporting activities, this role offers valuable experience that can accelerate long-term growth in Clinical Operations and Medical Affairs.
Candidates with strong clinical research foundations, monitoring expertise, and regulatory knowledge should strongly consider applying for this opportunity. Clinical Research remains one of the most stable and high-growth domains within the pharmaceutical industry, and positions like this can serve as stepping stones toward senior leadership roles in global clinical development programs.
Disclaimer
Note: Pharma Duniya does not charge any money for job information. Candidates are advised to verify details from the official company website.
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