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Location: Scotland, United Kingdom | Type: Remote | Country: GBClinical Research Associate (CRA II)Location:Remote, ScotlandTravel:Study dependent, typically 6-12 visits per month. DCT studies may require little to no on-site monitoring.Contract Type:Permanent, Full TimeBioTalent is supporting a growing CRO in the search for an experienced Clinical Research Associate to join its Clinical Operations team.Working across a mix of traditional, hybrid and decentralised clinical trials, you'll be responsible for managing investigator sites, building strong site relationships and ensuring studies are delivered to the highest quality standards.This is an excellent opportunity for a CRA looking for broad study exposure, a collaborative team environment and the flexibility of a remote-based role.Key ResponsibilitiesConduct Site Selection, Site Initiation, Monitoring and Close-Out VisitsPerform remote monitoring activities where requiredAct as the primary point of contact for assigned study sitesBuild and maintain strong relationships with investigators and site staffEnsure compliance with study protocols, ICH-GCP and regulatory requirementsReview source documents and verify data quality and integrityIdentify site issues and risks, implementing appropriate corrective actionsSupport site training, engagement and study performanceMonitor patient recruitment, retention and protocol complianceComplete monitoring reports and follow-up documentation within required timelinesCollaborate closely with Clinical Operations, Project Management and sponsor teamsMaintain accurate study documentation within CTMS and eTMF systemsRequirements3+ years' independent monitoring experience as a CRA within a CRO, biotech or pharmaceutical organisationExperience independently conducting SIVs, Routine Monitoring Visits and Close-Out VisitsStrong knowledge of ICH-GCP and clinical trial regulationsExperience managing multiple sites and studies simultaneouslyStrong communication and stakeholder management skillsExcellent organisational and problem-solving abilitiesAbility to work independently in a remote environmentFull right to work in the UKWillingness to travel as requiredDesirableExperience within decentralised (DCT) and hybrid clinical trialsExposure to biotech-sponsored studiesExperience using CTMS, eTMF and remote monitoring platformsBroad therapeutic area experienceWe're looking for a proactive, relationship-driven CRA who enjoys working closely with sites, takes ownership of their studies and can operate effectively in a remote environment.The successful candidate will be comfortable working independently, managing competing priorities and contributing to the successful delivery of innovative clinical trials across a diverse study portfolio.
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