CRA

A Leading CRO are seeking to appoint an experienced Clinical Research Associate who can work either office based in Oxfordshire, or home based. The Clinical Research Associate will be involved in setting up, feasibility studies, site monitoring, and on-site quality control of multi-centre, International clinical trials.
Main Responsibilities:

* Field Work: Preparation, conduct, and reporting of selection, initiation/start-up, routine/interim and closeout monitoring visits, Site management
* Communication and Training: Communication point for investigational sites, Back-up communication line for vendors and support services, On-site training of investigators and staff, Preparation and delivery of presentations at investigators' meetings
* Quality Control and Assurance: Supervised quality control of miscellaneous outbound documents, Preparation for and attendance at company audits
* Document Management: Liaison with sites on miscellaneous study documentation matters, Preparation and distribution of On-site Study Files to the sites
* Regulatory Affairs: Providing support to the Regulatory Affairs staff in procurement of site regulatory documents
* Data Management: Participation in query resolution, Maintenance of study-specific automated tracking systems
* Feasibility: Participation in feasibility research

Skills/Experience:

* Science/Life Science Degree
* Minimum 1 year independent UK monitoring experience
* Experience in regulatory submissions, contract negotiations, site management and feasibility assessment
* Recent CRA training, GCP training
* Previous oncology experience as a CRA is preferable
* Valid driver's license and ability to travel
* Proficient user of standard MS Office applications

This is a fantastic opportunity for the successful candidate to secure a permanent position within a reputable company.

To find out more about Real Staffing please visit www.realstaffing.com