Clinical Research Associate | Remote

1. Conduct site visits: Selection, Initiation, Monitoring, Close-out.
2. Prepare reports and follow-up letters for visits.
3. Manage site activities: Updates, Regulatory compliance, Material logistics, Document review, Safety events, Issue escalation.
4. Ensure GCP compliance and resolve audit findings.
5. Mentor associates for job growth.

Overview

• Industry - CRO, Clinical Research Organization
• Functional Area - Pharmacovigilence / Clinical Research
• Job Role - Clinical Research Associate/Manager
• Employment type - Full Time
• Work Mode - Remote

Qualifications

• Any Graduate - Any Specialization
• Any Post Graduate - Any Specialization
• Any Doctorate - Any Specialization

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