Description
The company in question are looking for experienced CRAs who are able to jump into the role, and take on some complex protocols. There's flexibility for the right candidates to work from home- but applicants must have the right to live and work within the UK.
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
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
