Sun Pharma Laboratories Ltd is recruiting a Clinical Research Associate (CRA) for its Clinical Research business unit. This exciting opportunity in clinical trials is based in Hyderabad, ideal for professionals with 1–5 years of experience in site management, monitoring, and GCP compliance.
Join Sun Pharma to “Create your own sunshine” in a supportive, growth-oriented environment focused on innovation and patient impact.
Contents
About the Company
Sun Pharmaceutical Industries Ltd (Sun Pharma) is one of India’s largest and most respected global pharmaceutical companies, specializing in generics, specialty medicines, APIs, and innovative formulations.
With a strong emphasis on R&D and clinical development, Sun Pharma conducts Phase III and Phase IV clinical trials to ensure high-quality, regulatory-compliant therapies reach patients worldwide.
The Clinical Research team plays a pivotal role in trial execution, site management, and data integrity. At Sun Pharma, employees are empowered to grow continuously, take ownership of their careers, and collaborate in a meritocratic, inclusive culture that values performance, creativity, and excellence.
Job Details
- Company Name: Sun Pharma Laboratories Ltd
- Position: Clinical Research Associate (Clinical Trials)
- Experience Required: 1–5 years minimum in clinical research
- Qualification: Bachelor’s or Master’s degree in a health-related field (e.g., Biology, Chemistry, Nursing, Pharmacy, Public Health) and/or Post-graduate Diploma in Clinical Research
- Location: Hyderabad (Sun House – Corporate Office / Clinical Research unit)
- Work Type: On-site / Hybrid (as per company norms for clinical roles)
- Business Unit: Clinical Research
Job Description
This CRA role involves end-to-end management of clinical trial sites, ensuring compliance with GCP, regulatory guidelines, and Sun Pharma’s policies. The position focuses on Phase III and Phase IV trials, site feasibility, monitoring, data quality, and stakeholder coordination.
Key Responsibilities
- Perform site feasibility assessments and identify potential investigators
- Negotiate study budgets, finalize investigators/sites, and execute CDAs/contracts
- Prepare and submit study documents for Ethics Committee (EC) approvals across centers
- Oversee Investigational Product (IP) dispensing, inventory management, and reconciliation
- Conduct timely site initiation, monitoring, and close-out visits; generate reports
- Train investigators and site personnel on study protocol, procedures, and GCP principles
- Ensure efficient participant recruitment, data entry, source data verification, and query resolution
- Report SAEs/SUSARs promptly and communicate to sites/investigators per regulations and PV policies
- Identify risks, analyze deviations, and implement CAPA for underperforming sites
- Coordinate with in-house teams or CROs for data management, statistical analysis, SAR, and database lock (DBL)
Skills & Qualifications Required
- Solid knowledge of GCP practices and regulatory guidelines in clinical trials
- Expertise in Phase III and Phase IV clinical trials
- Strong site management and monitoring skills
- Excellent collaboration with cross-functional stakeholders (e.g., data management, PV, CROs)
- Ability to handle documentation, risk assessment, and CAPA independently
- Effective communication, problem-solving, and organizational skills
- Relevant experience in clinical research (1–5 years)
Key Responsibilities (Summary)
- Site selection, feasibility, and contract negotiation
- EC submissions and regulatory compliance
- IP management and site training
- Monitoring visits, data verification, and query resolution
- SAE/SUSAR reporting and risk/CAPA management
- Coordination for data management and statistical activities
Benefits & Perks
- Robust opportunities for personal and professional growth
- Supportive community focused on continuous learning and career progression
- Emphasis on well-being, collaboration, and work-life balance
- Exposure to global clinical trials in a leading pharma innovator
- Competitive benefits package and recognition for performance
How to Apply
Apply directly through the official Sun Pharma Careers portal: careers.sunpharma.com
Search for “Clinical Research Associate” or similar listings in Hyderabad. Submit your updated resume and relevant documents.
Verified Post
Verification: To confirm the legitimacy of this posting, you can view the original announcement on the Sun Pharma Career page.
For more pharma jobs in clinical research, Hyderabad opportunities, and industry updates, visit Pharma Recruiter.
Your success matters—apply today and create your own sunshine at Sun Pharma!
Why Join Sun Pharma?
Sun Pharma fosters an empowering environment where you can grow daily, lead with confidence, and thrive together. Contribute to impactful clinical trials that advance healthcare, while enjoying stability, innovation, and a culture that prioritizes employee development and well-being in one of the world’s top pharmaceutical companies.
Frequently Asked Questions (FAQs)
What experience is required for the Clinical Research Associate role at Sun Pharma?
Minimum 1–5 years in clinical research, with expertise in site management, monitoring, and GCP.
What qualifications are needed?
Bachelor’s or Master’s in Biology, Chemistry, Nursing, Pharmacy, Public Health, or related fields; Post-graduate Diploma in Clinical Research is a plus.
Where is this CRA job located?
Hyderabad, in the Clinical Research business unit (corporate office environment).
Does Sun Pharma support career growth in clinical trials?
Yes—through continuous learning, challenging assignments, training, and a meritocratic culture focused on professional development.
