Research Associate

Freelance Clinical Research Associate (CRA) – Remote (UK-Based) Contract | Competitive Hourly Rate | Flexible Schedule I\’m working with a growing, full-service CRO that’s looking to bring an experienced Freelance CRA on board to support upcoming clinical trials. This is a small but expanding CRO that partners with biotech and pharma companies on early- to late-phase clinical trials. They’re known for being responsive, thorough, and committed to quality. As their study portfolio grows, they’re adding freelance CRAs to their network who can jump in and take ownership of site monitoring activities. Monitor clinical trial sites across various stages—site selection, initiation, routine monitoring, and close-out Review source data, CRFs, and site documentation for accuracy and completeness Work closely with the internal clinical project team to keep things moving smoothly At least 2 years of recent CRA experience in the U.Strong understanding of GCP, FDA regulations, and clinical trial processes Background in life sciences, nursing, or a related field (Bachelor’s degree required) Comfortable with EDC systems and remote monitoring tools S. with ability to travel regionally as needed (up to ~60%) Experience with women\’s health, Neurology and Medical device A flexible, problem-solving approach Competitive hourly pay Full remote flexibility + site travel Ongoing projects with potential for long-term collaboration