ARC Regulatory Ltd. in Belfast seeks a Clinical Site Monitor to visit and remotely assess in vitro diagnostic medical device clinical study sites, ensuring compliance with the study protocol, ICH GCP and local regulatory requirements.
The role involves qualification of sites, initiation, monitoring and close-out activities, and frequent collaboration with sponsors and ethics committees. Candidates should have a Life Sciences degree or equivalent, at least 5 years in Clinical Research with 3+
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Senior CRA - IVD Devices (Travel) employer: ARC Regulatory Ltd
ARC Regulatory is an exceptional employer for Pathologists, offering a flexible remote working environment across the UK and ROI, with occasional on-site attendance in Belfast. Our commitment to employee growth is reflected in our support for Continuing Professional Development, while our collaborative work culture fosters innovation in precision medicine and diagnostic services. Join us to be part of a team that values quality, compliance, and meaningful contributions to global clinical trials.
