Description
Job Role
* Performing all types of site visits (feasibility, site selection, interim and close-out) in accordance with the clinical monitoring plan
* Fostering effective relationships with investigator site staff
* Increasing site and patient recruitment
* Proactively and promptly implementing corrective action plans, and, when applicable, escalates issues to more senior members of the study team
* Designing and delivering training to site staff, when appropriate.
* Preparing for and attending investigator meetings
* Coordinating the timely shipment and the subsequent proper storage and accountability of clinical supplies
* Willingness to monitor nationally
Preferred Requirements
* Education - BSc/BA or equivalent
* Experience working in pharmaceutical or CRO environment
* Strong communication and interpersonal skills
* Excellent computer skills
* Valid UK driving license
