- Monitor clinical trial sites to ensure compliance with study protocols, SOPs, GCP, and regulatory requirements.
- Conduct site initiation, interim monitoring, and close-out visits.
- Act as the primary contact between sponsor/CRO and study sites.
- Train investigators and site staff on protocol, CRFs, and study procedures.
- Ensure timely enrollment, data entry, and query resolution.
- Prepare monitoring visit reports and follow-up letters.
- Track study progress, timelines, and site performance.
- Collaborate with data management, medical, and regulatory teams
[email protected] (phone hidden)
Working Hours -10:00 -7:00 pm
Job Types: Full time, Permanent
Pay: ₹13,000.00 - ₹15,000.00 per month
Work Location: In person
📌 Customer Relation Associate (Kannur)
🏢 Therefore I'm
📍 Kannur