Customer Relation Associate

• 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]

9048416565

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