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
hr@thereforeim.com
9072349800
Females preferred
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
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