Clinical Research Associate - Freelance

Clinical Research Associate - Freelance

TFS HealthScience

Remote, United Kingdom

Key Responsibilities

• 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

Qualifications

• 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