Clinical Research Associates – LATVIA
We are currently looking for a talented to work for us in the Co-source department as our sponsor, a well-known pharma company, is currently expanding their Clinical Operations team. The role is full-time/permanent and the succesful candidate will be office-based at Client's in Riga.
This is a CRA position available to work within our Phase II-IV CoSource division directly with pharmaceutical company. As an experienced CRA you’ll be involved in initiation, routine & close out visits concentrating on sites in Latvia..
As a CRA you will manage all aspects of study site monitoring according to SOPs, GCP, and ICH guidelines, including pre-study qualification and initiation visits, routine monitoring, close-out of clinical sites, and maintenance of study files.
At Covance, you will join like-minded professionals who, together, build our reputation as one of the world's largest and most respected contract research organizations. In choosing Covance, you will be part of a dedicated team that makes a difference in helping to deliver life-saving and life-enhancing medicines to people around the world.
We welcome your application and believe this decision may be the most rewarding career move you will ever make!