Clinical Research Associate Job at Sun Pharma in Hyderabad
Sun Pharma Laboratories Ltd is offering an exciting clinical research associate job for professionals looking to grow in regulated clinical trials. This opportunity under Sun Pharma careers allows candidates to work in a structured clinical research environment while contributing to high-impact Phase III and Phase IV studies, with career exposure comparable to top pharma roles and jobs in Mumbai and other metro locations.
Clinical Research Associate Job Details:
- Job Position: Clinical Research Associate
- Business Unit: Clinical Research
- Location: Hyderabad
About the Company
Sun Pharma Laboratories Ltd is one of India’s leading pharmaceutical companies, offering strong career growth through structured roles in clinical research and drug development. Known globally for quality and innovation, Sun Pharma careers offer professionals opportunities similar to those at leading pharma organizations, with jobs in Mumbai, Hyderabad, and other major research hubs.
Qualifications
Bachelor’s or Master’s degree in a health or related field, or in Public Health
Clinical Research Associate Job Description
This job focuses on end-to-end management of clinical trial activities, ensuring compliance with GCP, regulatory requirements, and study protocols. The role involves close coordination with investigators, CRO partners, and internal stakeholders, offering exposure comparable to advanced Sun Pharma careers and other leading pharma jobs in Mumbai.
Key Responsibilities:
- Perform site feasibility, identify potential investigators, negotiate study budgets, finalize investigators and sites, and execute CDA and study-related contracts.
- Prepare and submit study documents for EC permission for respective studies across centers
- Oversee and document IP dispensing, inventory management, and reconciliation.
- Ensure timely site initiation, monitoring, and close-out activities, with appropriate report generation.
- Train investigators and site personnel on study protocol, procedures, and GCP principles.
- Ensure timely recruitment of trial participants and efficient data entry, source data verification, and query resolution
- Ensure timely reporting of SAEs and SUSARs in accordance with regulations and Sun Pharma PV policies.
- Conduct risk identification, analysis, and CAPA for sites that do not meet expectations.
- Coordinate with in-house teams or CRO partners for data management, statistical analysis, statistical analysis reports, and database lock.
