Clinical Trial Monitor
- This new and exciting project will be to provide support to the implementation of the clinical research operations programme for all appropriate therapeutic areas for our clients Medical Devices in accordance with all applicable regulations for Medical Devices
- Other duties will include planning & implementing a programme of monitoring for all international regulatory and post marketing clinical research studies and maintain the highest ethical, clinical and scientific standards ensuring both the safety and well being of all trial participants, and good/rigorous scientific practice
Relevant experience in implementation of clinical research studies.
Working knowledge of international regulatory requirements applicable to clinical research and awareness of research ethics.
Candidates wishing to apply will need to have above average oral, written and communicative skills.
If this is of interest to you, please get in touch and apply today!
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