Our client is a name that everyone in Medical Devices in Ireland knows. They are undergoing development which includes team expansion and the need for a Director to lead the strategic direction of this business unit which is focused on MDR.
This role is responsible for the clinical assessment and scientific review of technical compliance (including pre-clinical data, clinical data, trial data, market evaluation data, user instructions, and risk management documentation) for In Vitro Diagnostic Medical Devices.
To be considered, you must be a registered medical practitioner with IMC with at least four years post-graduate experience including direct patient care. Knowledge of clinical research and experience in the assessment of clinical trials is required.
It is a senior position and interest is invited from clinically qualified professionals.
Contact Adam directly for a Confidential discussion via videocall which can be in or outside of normal office hours.
Clinical Evaluator – In Vitro Diagnostics Devices
Ireland: Hybrid inc Dublin Office
Remuneration: circa €90k – €102k