Clinical Research Associate Jobs at Sun Pharma | Chemistry Grads Apply
Are you looking for Clinical Research Associate jobs in a leading pharmaceutical organization? Sun Pharma Laboratories Ltd is offering an excellent opportunity for experienced clinical research professionals to join its Clinical Research team in Hyderabad. This role is ideal for candidates seeking long-term growth through Sun Pharma Jobs, where innovation, responsibility, and collaboration drive success in global clinical trials.
- Job Title: Clinical Research Associate
- Location: Hyderabad
- Business Unit: Clinical Research
About Sun Pharma
Sun Pharma Laboratories Ltd is India’s largest pharmaceutical company and a trusted global leader in specialty generics. Known for innovation, compliance, and patient-centric research, Sun Pharma Careers offers professionals an opportunity to work on impactful healthcare solutions. With a strong presence in clinical research and trials, Sun Pharma Jobs provide long-term growth, learning, and exposure to global regulatory standards.
Key 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.
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.
