Sun Pharmaceutical Industries Ltd. has announced a Clinical Research Associate (CRA) hiring opportunity for 2026 in its Clinical Research Business Unit located in Hyderabad.
This role is ideal for professionals with 1–5 years of clinical research experience, particularly those skilled in site monitoring, GCP compliance, and clinical trial coordination. Candidates interested in contributing to global clinical trials and regulatory-compliant research will find this opportunity highly rewarding.
About Sun Pharma
Sun Pharmaceutical Industries Ltd., commonly known as Sun Pharma, is one of the largest pharmaceutical companies in India and among the top global generic drug manufacturers.
Founded in 1983, the company operates in more than 100 countries and focuses on:
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Generic medicines
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Specialty pharmaceuticals
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Active Pharmaceutical Ingredients (APIs)
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Innovative formulations and drug delivery systems
Sun Pharma maintains a strong research and development ecosystem, conducting Phase III and Phase IV clinical trials to ensure medicines meet international safety and efficacy standards.
The organization promotes a collaborative and performance-driven culture, encouraging employees to “Create Your Own Sunshine” through continuous growth and innovation.
Job Details
Company: Sun Pharma Laboratories Ltd
Position: Clinical Research Associate (CRA)
Business Unit: Clinical Research
Location: Hyderabad
Experience Required: 1–5 years
Qualification: Bachelor’s or Master’s degree in a health-related field
Work Type: On-site / Hybrid (depending on trial requirements)
Role Overview
The Clinical Research Associate (CRA) will be responsible for managing clinical trial sites and ensuring compliance with regulatory standards throughout the clinical study lifecycle.
The role involves site monitoring, investigator coordination, documentation management, and data verification, helping ensure that clinical trials produce reliable and regulatory-compliant results.
Key Responsibilities
Clinical Trial Site Management
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Conduct site feasibility assessments and select qualified investigators
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Manage study budgets and execute investigator agreements
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Coordinate site initiation and close-out activities
Regulatory & Ethics Compliance
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Prepare and submit documentation for Ethics Committee approvals
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Ensure adherence to ICH GCP Guidelines
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Maintain regulatory compliance throughout the trial lifecycle
Monitoring & Data Integrity
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Perform site monitoring visits and prepare monitoring reports
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Conduct Source Data Verification (SDV) to ensure data accuracy
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Manage queries and maintain high data quality standards
Safety Monitoring
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Report Serious Adverse Events (SAEs) and Suspected Unexpected Serious Adverse Reactions (SUSARs)
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Coordinate safety reporting with pharmacovigilance teams
Cross-Functional Collaboration
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Work closely with data managers, statisticians, and trial managers
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Coordinate activities with Contract Research Organizations (CROs)
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Support database lock (DBL) and final clinical study reporting
Skills & Qualifications Required
Candidates applying for this role should possess:
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1–5 years of clinical research experience
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Strong knowledge of Good Clinical Practice (GCP) guidelines
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Experience in Phase III and Phase IV clinical trials
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Site management and monitoring expertise
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Strong documentation and compliance skills
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Ability to identify risks and implement Corrective and Preventive Actions (CAPA)
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Excellent communication and stakeholder management abilities
A Postgraduate Diploma in Clinical Research will be an added advantage.
Benefits of Working at Sun Pharma
Joining Sun Pharma provides exposure to global clinical development programs and advanced pharmaceutical research environments.
Key Benefits
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Opportunities to participate in international clinical trials
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Structured learning and professional development programs
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Collaborative and inclusive workplace culture
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Competitive compensation and benefits package
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Strong focus on employee well-being and work-life balance
Employees gain valuable experience working with one of the largest pharmaceutical R&D ecosystems in India.
How to Apply
Candidates interested in this opportunity can apply through the official careers portal of Sun Pharmaceutical Industries Ltd..
Application Steps
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Visit the official career portal
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Search for Clinical Research Associate – Hyderabad
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Submit your updated resume and supporting documents
Official careers page:
https://careers.sunpharma.com
Clinical Research Associate Roles in Pharma
Clinical Research Associates play a crucial role in ensuring that clinical trials are conducted ethically, safely, and in compliance with global standards.
Regulatory authorities such as the:
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U.S. Food and Drug Administration
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International Council for Harmonisation
require strict adherence to clinical trial protocols, safety monitoring, and accurate data reporting.
CRAs serve as the link between clinical trial sites, sponsors, investigators, and regulatory authorities, ensuring the successful execution of clinical studies.
Why Join Sun Pharma?
Sun Pharma offers a unique environment for professionals looking to grow in clinical research and pharmaceutical innovation.
Key Advantages
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Exposure to large-scale global clinical trials
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Opportunity to work with experienced clinical research professionals
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Continuous learning and career development opportunities
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Impactful work contributing to patient safety and healthcare innovation
Working with Sun Pharma allows professionals to build a strong career in clinical development, regulatory science, and pharmaceutical research.
Frequently Asked Questions (FAQs)
What experience is required for the CRA role?
Candidates should have 1–5 years of clinical research experience, particularly in site monitoring and GCP compliance.
What qualifications are required?
Bachelor’s or Master’s degree in Biology, Pharmacy, Chemistry, Nursing, Public Health, or related healthcare fields. A Postgraduate Diploma in Clinical Research is advantageous.
Where is the job location?
The role is based in Hyderabad, Telangana, India.
Does Sun Pharma offer career growth in clinical research?
Yes. Sun Pharma provides continuous training, learning programs, and career development opportunities for clinical research professionals.