25 January, 2023
Sun Pharma Hiring Senior Executive – Clinical Research Associate
Perform evaluation of sites and monitor clinical trial data to ensure compliance to clinical trial study protocol, ICH-GCP and regulations. Ensure subjects’ rights, safety and wellbeing.
What are the key responsibility of the role?
- Identification of potential sites for studies.
- Coordination with Clinical sites, vendors and internal stakeholders.
- Conducting site assessment through feasibility and site qualification visit.
- Provide training and guidance to sites throughout the study.
- Perform monitoring visits at participating sites and review data and ensure compliance and subject safety and wellbeing.
- Preparing the report, supporting the PM in drafting the plans, collection of information, adherence to study timelines
M.Pharm, / MSc
4 years in related field
Skills / Competencies
1. Computers, proficiency in word and excel, exp. Of working with clinical trial systems like ctms, edc, etc.