Clinical Research Job at Sun Pharma | Clinical Research Associate | M Pharmacy Graduates
If you are searching for a Clinical Research Job in the pharmaceutical industry, this latest opportunity at Sun Pharmaceutical Industries Ltd could be ideal for your career growth. The company is hiring a Clinical Research Associate (Clinical Trials) in Hyderabad for professionals with experience in clinical trials and regulatory processes. This Pharma Job offers candidates the chance to work in clinical research operations, site monitoring, and trial management while contributing to global drug development.
- Job Title: Clinical Research Associate
- Location: Hyderabad, Sun House – Corporate Office
About the Company
Sun Pharmaceutical Industries Ltd is one of the world’s leading specialty generic pharmaceutical companies headquartered in India. The company focuses on delivering high-quality medicines and advancing healthcare through innovation, research, and global clinical development programs.
Job Description
This Clinical Research Job involves managing clinical trial sites, coordinating with investigators, and ensuring compliance with Good Clinical Practice (GCP) and regulatory guidelines.
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 Sun’s 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.
Qualification
Bachelor’s or Master’s degree in Pharmacy 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.
