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Clinical Research Associate (CRA)
Next Code Placement
UK | United Kingdom
Not Disclosed
1 - 5 Years
Full Time - Permanent
Views:16
Applicants:0
Posted on 7 Oct, 2026
In Office
Job Description | Responsibilities
- Monitor clinical trials to ensure protocol and regulatory compliance.
- Conduct site visits and review trial documentation.
- Verify data accuracy, patient records, and study procedures.
- Communicate with investigators, sponsors, and clinical teams.
- Track study progress, issues, and corrective actions.
Overview
- Industry - HR / OD / L&D / Training / Counselling / Coaching Firms, CRO, Clinical Research Organization
- Job Role - Clinical Research Associate (CRA)
- Employment type - Full Time - Permanent
- Work Mode - In Office
Qualifications
- Any Graduate - Any Specialization
- Any Post Graduate - Any Specialization
- Any Doctorate - Any Specialization
Job Related Keywords
Clinical Research
Clinical Trials
GCP
Site Monitoring
Regulatory Compliance
Clinical Data
Protocol Management
EDC
