Clinical Research Associate Job at Sun Pharma | Pharmacy Graduates Apply Now
Sun Pharma Laboratories Ltd. is hiring a Clinical Research Associate (CRA) to join its Clinical Research Business Unit, based at the Corporate Office in Hyderabad. This Clinical Research Associate Job requires a Bachelor’s or Master’s degree (Pharmacy, Nursing, or related field) and 1-5 years of relevant experience in Clinical Research. The CRA will oversee critical site management activities, including investigator finalization, site monitoring, IP reconciliation, and ensuring strict compliance with GCP principles. Expertise in Phase III and Phase IV Clinical Trials and timely reporting of SAEs/SUSARs are essential for this role.
- Job Title: Clinical Research Associate (Clinical Trials)
- Location: Sun House – Corporate Office, Hyderabad
About The Company
Sun Pharma Laboratories Ltd. is a subsidiary of Sun Pharmaceutical Industries Ltd., a multinational pharmaceutical company and one of the largest in India, with a significant global presence. Sun Pharma is committed to providing affordable, high-quality medicines and driving innovation. The company’s Clinical Research unit operates under stringent compliance standards, focusing on accelerating drug development across various phases. Sun Pharma emphasizes a culture of continuous growth, self-drive, and collaboration, encapsulated by its philosophy “Create your own sunshine,” to make a lasting impact on global health.
Key Responsibilities of the Pharmacy Job
- Perform site feasibility, identify potential investigators, negotiate study budget with potential investigators, finalize of 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
Educational Qualification
Bachelor’s or Master’s degree in a health or related field, such as Pharmacy/or Post-graduate Diploma in Clinical Research
Experience required for the Pharmacy Job
Relevant experience of 1-5 years minimum in the field of Clinical Research.
Additional Skills
- Knowledge of GCP practices, regulatory guidelines in Clinical Trials
- Phase III and Phase IV Clinical Trials knowledge expertise
- Site Management expertise
- Collaboration with cross-functional stakeholders
