Clinical Research Associate
2 weeks ago
Check out the role overview below If you are confident you have got the right skills and experience, apply today.
Responsibilities:
- Conduct site qualification, initiation, monitoring, and closeout visits
- Ensure compliance with protocols, regulatory requirements, and GCP guidelines
- Perform source data verification and review study documents
- Track and report patient enrollment and study progress
- Communicate with study sites and investigators
Requirements
Requirements: - Bachelor's degree in a health-related field or equivalent
Benefits
Excellent salary and benefits package Encourages work life balance Car allowance
Whatever your career goals, my client is here to ensure you get there If you are an experienced CRA looking for a new and exciting opportunity then please get in touch To apply, please submit your resume at:
E: jordan@alsolutions.co.uk
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