Clinical Research Associate Jobs at SunPharma | MSc Chemistry Candidates Apply
Clinical Research Associates Jobs at SunPharma. Are you ready to accelerate your career in clinical research? Sun Pharma Laboratories Ltd is hiring a Clinical Research Associate (CRA) for its Clinical Research division in Nagpur. In this role, you’ll oversee site feasibility, budget negotiations, GCP-based site monitoring, safety reporting, and cross-functional coordination—playing a pivotal part in advancing life-saving clinical trials. Interested candidates apply at Sun Pharma Careers.
Company Overview:
At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community.
- Job Title: Clinical Research Associate
- Business Unit: Clinical Research
- Location: Nagpur
Key Responsibilities:
- Perform site feasibility, identify potential investigator, negotiate study budget with potential investigators, finalization of investigators, sites, and execution of CDA and study-related contracts.
- Preparation and submission of study documents for EC permission for 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 Masters 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.
