Sun Pharma Hiring for Clinical Research Associate Role – BS & MS Biology Graduates Apply Now

Clinical Job at Sun Pharma – Jobs in Bangalore | Biology Graduates Apply Now

Looking for a rewarding Clinical Job at Sun Pharma? Here’s your opportunity to join one of India’s most trusted pharmaceutical companies as a Clinical Research Associate in Bangalore. This dynamic position offers hands-on experience in clinical trials, regulatory compliance, and site management. If you’re passionate about driving innovation in healthcare, explore one of the best jobs in Bangalore with Sun Pharma, where you can create your own sunshine and grow every day.

• Job Position: Clinical Research Associate
• Business Unit: Clinical Research
• Location: Bangalore
• Company: Sun Pharma Laboratories Ltd

About the Company:

Sun Pharma Laboratories Ltd is a global leader in pharmaceuticals, known for innovation, integrity, and excellence in healthcare. With a mission to empower employees to “Create your own sunshine,” Sun Pharma provides an environment that nurtures growth, collaboration, and continuous learning. Join the team and explore fulfilling jobs in Bangalore that let you make a meaningful impact on patients lives.

Qualifications:

• Bachelor’s or Master’s degree in Biology or a related field.
• Postgraduate Diploma in Clinical Research preferred.
• Minimum 1-5 years of experience in the clinical research domain.
• Sound knowledge of GCP, regulatory practices, and site management.
• Experience in Phase III and IV Clinical Trials.
• Strong collaboration and communication skills across functional teams.

Job Description:

This Clinical Job at Sun Pharma offers an exciting opportunity to work as a Clinical Research Associate (CRA) in the Clinical Research business unit. You’ll be responsible for executing and managing clinical trials, ensuring regulatory compliance, and maintaining high-quality data. This role is ideal for professionals passionate about clinical research, site management, and operational excellence.

Key Responsibilities:

• Perform site feasibility and identify potential investigators.
• Negotiate study budgets, finalize investigators, and manage site contracts.
• Prepare and submit study documents for EC permissions across centers.
• Oversee IP dispensing, inventory management, and reconciliation.
• Conduct site initiation, monitoring, and close-out activities.
• Train investigators and site personnel on study protocols and GCP compliance.
• Ensure efficient participant recruitment, data verification, and resolution of queries.
• Report SAEs and SUSARs, ensuring alignment with regulatory and PV guidelines.
• Identify site-related risks and implement CAPA for performance improvement.
• Coordinate with internal teams and CROs for data management and analysis.

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