Freelance Clinical Research Associate

Job Summary

A company is looking for a freelance Clinical Research Associate (CRA).

Key Responsibilities

• Conduct and report on all types of monitoring visits, including site selection and close-out visits
• Coordinate and lead monitoring activities autonomously, advising Trial Managers on process improvements
• Collaborate with tech and product teams to enhance the Citrus trial monitoring platform

Required Qualifications

• 3+ years of independent site monitoring experience
• Experience with Decentralized Clinical Trials (DCT) and central monitoring approaches
• Strong knowledge of GCP/GDP and regulatory requirements
• Ability to develop and review monitoring plans with a risk-proportionate approach
• Experience in a startup or early-stage environment is advantageous