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Job Title


Clinical Research Associate


Company : Home Recruitment Ltd


Location : Birmingham, West Midlands


Created : 2025-06-20


Job Type : Full Time


Job Description

International Clinical Research Specialist Cardiology Medical Device TrialsRead all the information about this opportunity carefully, then use the application button below to send your CV and application.Join a medical device start-up advancing next-generation cardiac technologies through breakthrough innovation and global clinical research. With a growing European trial programme, the company is hiring an International Clinical Research Specialist to support study execution across multiple countries.Role OverviewThis fully field-based role is ideal for a clinical research professional with strong GCP knowledge and hands-on experience in medical device clinical trials. Working across Europe, youll play a critical role in ensuring protocol adherence, site compliance, and smooth operational delivery in partnership with CROs and internal global teams.Extensive travel across Europe is required | Experience with medical device trials is required.Key ResponsibilitiesServe as the main point of contact for assigned research sites across EuropeSupport site start-up, initiation, monitoring, and close-out activities in line with study plansEnsure compliance with GCP, ISO 14155, and local regulatory requirementsCollaborate with investigators, study staff, CROs, and internal stakeholders to ensure high-quality executionMonitor data accuracy and assist with query resolution and EDC trackingOversee device logistics, including shipments, returns, and clinical inventoryManage essential documents and site binders to maintain audit readinessProvide ongoing study updates and contribute to data tracking and reportingCandidate ProfileMinimum 2 - 4 years experience in clinical research, specifically involving medical devicesStrong understanding of ICH-GCP, ISO 14155:2020, and European clinical trial regulationsExperience working with CROs and supporting multi-country site managementFamiliarity with electronic data capture (EDC) and clinical trial management systemsExcellent communication and organisational skills with strong attention to detailFluent in English; additional European languages are an assetSelf-motivated and flexible, with the ability to travel extensively across EuropeImportant: We are only able to consider candidates with clinical trial experience in medical devices. Applications from candidates with only pharmaceutical experience will not be considered.If you're ready to join a mission-driven team transforming cardiac care, apply now to be part of a high-impact team!