Sun Pharma Careers: Clinical Research Associate | Chemistry Graduates Apply Now
Are you looking for Clinical Research Associate opportunities in Hyderabad with a leading pharmaceutical company? Sun Pharma Careers offers an exciting role for a Clinical Research Associate (Clinical Trials) in its Clinical Research Business Unit. This is an excellent opportunity and is ideal for professionals seeking growth in clinical trials, regulatory compliance, and site management, while also opening pathways for long-term Chemistry Careers in the pharmaceutical and research industry.
About Sun Pharma
Sun Pharma Laboratories Ltd is one of the world’s leading pharmaceutical companies, committed to delivering high-quality and affordable medicines across global markets. Through Sun Pharma Careers, professionals are empowered to build meaningful roles in research, manufacturing, regulatory affairs, and global operations. The organization actively supports Chemistry Careers in formulation development, analytical research, and drug innovation, while also offering dynamic growth paths for a Clinical Research Associate within its Clinical Research division.
- Job Title: Clinical Research Associate (Clinical Trials)
- Location: Hyderabad
- 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.
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 forthe 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
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
