Freelance Clinical Research Associate

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