SCRA

We are seeking Senior Clinical Research Associates to work on projects for major Pharmaceutical Companies across the UK and Europe. The successful SCRA can be either office based or home based. Our client offers excellent career progression and competitive salaries.

Main Responsibilities (to include but not be limited to):

* Responsibility for site administration and coordination including oversite of Ethics Committee submissions, data resolution, drug accountability, site agreement finalisation

* Responsibility for monitoring of sites in accordance with Client SOPs, ICH Guidelines, and GCP.

* Responsibility for the quality of the data for those sites for which he or she is assigned in an oversight role

* Site management may be required

* Assuring the Project Plans are implemented and carried our accordingly

* Assume Line Management duties as and when is required
* A Senior CRA may also participate in Group process improvement activities including revision of SOPs, in mentoring junior staff and performing national coordination of clinical projects

Skills/Experience:

* Degree educated in a Science/Life Science discipline

* Minimum of 2 years experience as a Clinical Research Associate with experience monitoring across multiple sites

* Experience working within Diabetes, MS, and/or Oncology therapy areas is advantageous
* Fluent in spoken/written English

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

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