SESeven Consultancy
Clinical Research associate
Bangalore ₹5-8 LPA Posted 12 Dec 2025
FULL TIME
Analysis
Clinical Trials
Clinical Data Management
Clinical Research
Recruitment
Job Description
- Create and write trial protocols and present them to the steering committee.
- Identify, evaluate, and establish trial sites, and close sites upon trial completion.
- Train site staff on therapeutic areas, protocol requirements, proper source documentation, and case report form completion.
- Liaise with ethics committees regarding the rights, safety, and well-being of trial subjects.
- Order, track, and manage investigational products (IP) and trial materials.
- Oversee and document IP dispensing, inventory management, and reconciliation.
- Protect subject confidentiality, update information, and verify that IP has been dispensed and administered according to protocol.
- Conduct regular site visits, coordinate project meetings, and write visit reports.