Clinical Research Associate – Freelance
United Kingdom
Part Time
13 hours ago
No Sponsorship
Key skills
Google Cloud PlatformGCPGoogle CloudCommunicationCollaboration
About this role
Role Overview
- Perform on-site and remote monitoring visits
- Ensure protocol compliance, patient safety, and data integrity
- Review CRFs and source data for accuracy
- Verify informed consent procedures are followed
- Manage investigational product accountability
- Write and submit monitoring visit reports
- Track issues and ensure timely follow-up with sites
- Maintain eTMF/ISF documentation compliance
- Support audits and inspections
- Update CTMS and study systems with accurate data
Requirements
- Bachelor’s degree in Life Sciences, Nursing, or similar
- 3+ year clinical research experience or relevant academic experience
- Knowledge of GCP, ICH, and clinical trial processes
- Strong communication and organizational skills
- Ability to work independently and in teams
- Fluent in English
- Experience in CNS/Neuro studies is a big advantage
Tech Stack
- Google Cloud Platform
Benefits
- Opportunities for personal and professional growth
- Rewarding environment
- Team that values collaboration, quality, and making a difference in patients' lives