ARC Regulatory in Belfast is looking for a Clinical Lead to drive the delivery of clinical research projects in compliance with stringent protocols. The role involves managing study design, coordinating with stakeholders, and ensuring compliance with regulatory requirements. Candidates should possess a degree in biological sciences and at least 3 years of clinical experience in IVD device manufacturing. The ideal candidate has expertise in regulatory standards, project management, and document authoring, offering a dynamic opportunity to contribute to precision medicine.
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