Clinical Research Associate Jobs at Sun Pharma | MSc Chemistry Candidates Apply
Clinical Research Associate Jobs. A career as a Clinical Research Associate at Sun Pharma offers an excellent opportunity to work at the forefront of clinical trials, patient safety, and regulatory compliance. Based in Hyderabad, this role plays a critical part in site management, investigator coordination, data integrity, and Phase III and IV clinical trial execution. With intense learning exposure and a growth-driven culture, Sun Pharma provides a dynamic platform for clinical research professionals to thrive and make a real-world impact. Interested candidates apply for the exciting opportunity at Sun Pharma Careers.
Company Overview:
As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.
- Job Title: Clinical Research Associate (Clinical Trials)
- Date: Dec 6, 2025
- Location: Sun House – Corporate Office, Hyderabad
- Business Unit: Clinical Research
Key Responsibilities:
- Perform site feasibility, identify potential investigators, negotiate study budget with potential investigators, finalize investigators, sites, and execute CDA and study-related contracts
- Preparation and submission of study documents for EC permission for the respective study across centers
- Oversee & document IP dispensing, inventory management & reconciliation
- Ensure timely site initiation, site monitoring, and site close-out activities are performed, and respective reports are generated
- Investigator and site personnel training on the Study protocol, procedures, and GCP principles
- Ensure timely recruitment of trial participants and subsequent efficient and effective data entry, source data verification, and query resolution
- Ensure timely reporting of SAEs, SUSARs, and reporting of SAEs to all sites and investigators in alignment with regulations and Sun’s PV policies
- Risk identification, analysis, and CAPA for sites not meeting expectations as per the plan
- Coordinate with in-house or CRO partners for data management, statistical analysis, statistical analysis report & DBL
Job Requirements:
Educational Qualification:
Bachelor’s or Master’s degree in a health or related field, such as Biology, Chemistry, Nursing, Pharmacy, or Public Health, and/or Post-graduate Diploma in Clinical Research
Experience:
Relevant experience of 1-5 years minimum in the field of Clinical Research.
Additional Skills:
- Knowledge of GCP practices and regulatory guidelines in Clinical Trials
- Phase III and Phase IV Clinical Trials knowledge expertise
- Site Management expertise
- Collaboration with cross-functional stakeholders
