The post holder will take responsibility for the overall set up, coordination and data management of clinical trials supporting and facilitating both academic and commercial clinical trials alongside a lead research nurse. The set up process and Quality Assurance are key aspects of this post. They will serve as the main contact point for all internal and external parties involved in set up, maintenance and close down of all clinical trials within their portfolio. They will be responsible for coordination of clinical trials, for the team, and also have a role in recruiting patients into clinical trials ensuring that all trial protocols are adhered to.
The post holder will be familiar with ICH/GCP, and have good all round clinical trial management skills. Excellent IT skills with a working knowledge of Microsoft Office software are essential. You should be enthusiastic, and possess excellent communication, negotiation and organisational skills. Working autonomously, using your own initiative as well as possessing strong team working skills and an ability to motivate staff is essential.
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