As a clinical research specialist you will not only be involved in monitoring clinical trials across the region you are responsible for, you will also be involved in coordinating the trials and selecting and nominating sites where trials could be conducted.
Using your previous monitoring and coordinating experience of clinical trials you will have responsibility for site selection, recruitment and the implementation of study protocol. You duties will also include acting as the key member in the liaison between the sites. This is a perfect opportunity to develop managerial and leadership skills setting you on the path to future career progression. With sites across Europe you can build on your international experience opening up employment prospects with other global corporations.
Successful candidates will have had previous experience in the monitoring and coordination of European clinical trials.
To discuss this opportunity or others in this market please contact Toby Drewitt on +44 (0)207940 2105 or email t.drewitt@nonstop-recruitment.com
