Beta Release
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Posted on 15 Mar, 2024
Job Description | Role and Responsibilities
- Conduct site visits: Selection, Initiation, Monitoring, Close-out.
- Prepare reports and follow-up letters for visits.
- Manage site activities: Updates, Regulatory compliance, Material logistics, Document review, Safety events, Issue escalation.
- Ensure GCP compliance and resolve audit findings.
- 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
Job Related Keywords
Education
- Any Graduate - Any Specialization
- Any Post Graduate - Any Specialization
- Any Doctorate - Any Specialization
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