HIRANI is seeking a Clinical Site Monitor to oversee in vitro diagnostic device clinical studies, ensuring protocol adherence, ICH-GCP, and local regulatory compliance. The role involves site qualification, initiation, monitoring, and close-out across study sites, with both on-site and remote activities.
The ideal candidate has 5+ years in Clinical Research, including 3+ years monitoring medical device/IVD trials, and strong data verification skills along with GCP/GLP auditing experience.
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Senior Clinical Research Associate - IVD/Medical Device employer: HIRANI
HIRANI is an exceptional employer located in Belfast, offering a dynamic work culture that fosters innovation and collaboration in the healthcare sector. Employees benefit from comprehensive professional development opportunities and a supportive environment that encourages growth and creativity, making it an ideal place for those passionate about leveraging Data and AI to drive meaningful change in healthcare.
