(SCRA) – UK (6–8 Site Visits/Month) - Global CROMy client is a leading global Contract Research Organization (CRO), trusted by top pharmaceutical and biotech companies worldwide to deliver high-quality clinical research solutions. They are committed to advancing human health through innovation, collaboration, and scientific excellence.The Opportunity On behalf of my client, I am seeking an experienced Senior Clinical Research Associate (SCRA) to join their UK team. This position offers a balanced workload of 6–8 site visits per month, giving candidates the chance to work on impactful global studies while maintaining a sustainable travel schedule.Key ResponsibilitiesConduct routine on-site monitoring visits in line with ICH-GCP, UK regulations, and sponsor SOPs.Develop and maintain strong site relationships to ensure high standards of performance and compliance.Perform source data verification (SDV), CRF review, and essential document checks.Identify and resolve site or protocol-related issues, escalating where required.Act as a resource and mentor for junior CRAs as needed.Candidate ProfileMinimum of 18–24 months’ independent monitoring experience as a CRA.Strong knowledge of ICH-GCP guidelines and UK regulatory environment.Multi-therapeutic area experience advantageous.Excellent communication, organizational, and problem-solving skills.Life sciences degree (or equivalent).Willingness to travel across the UK (6–8 site visits per month).What’s on OfferCompetitive salary and comprehensive benefits package.Flexible home-based working.Career progression opportunities within a global CRO.Supportive, collaborative working environment.
Job Title
Senior Clinical Research Associate