Sun Pharma Careers: Clinical Research Associate | Apply Now
Are you looking for Clinical Research Associate opportunities in Mumbai with a reputed pharmaceutical leader? This exciting role under Sun Pharma Careers offers hands-on exposure to clinical trial management, regulatory coordination, and investigator engagement. Ideal for professionals exploring MSc Chemistry Jobs or health-science careers, this Clinical Research Associate position provides strong growth potential in clinical operations, GCP compliance, and global research standards.
About Sun Pharma
Sun Pharma Laboratories Ltd is a leading pharmaceutical company dedicated to innovation and excellence in the healthcare sector. We focus on bringing world-class products to enhance patient care. With a commitment to research and development, we strive to make a significant impact on global health.
- Job Title: Clinical Research Associate
- Job Location: Mumbai
- Qualification: Minimum qualification requirement is to have a Bachelor’s or Master’s degree in a health-related field, such as Biology, Chemistry, Nursing, Pharmacy, or Public Health, and/or a Post-graduate Diploma in Clinical Research
- Experience: Relevant experience of 1-5 years minimum in the field of Clinical Research
Responsibilities
- Perform site feasibility, identify potential investigators, negotiate study budget with potential investigators, finalize the investigators, sites, and execution of 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 Suns 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
