There is a fantastic opportunity to join an expanding CRO, who are looking for an experienced CRA II to join their team out in Belgium or the Netherlands. This is a role that will expect around 2-4 monitoring visits, with the remainder being homebased.
About the Company.
They are an exciting and innovative CRO who are growing throughout Europe. They provide a specialist and responsive service to clients globally, across a wide variety of therapeutic areas. Having been established over three decades ago, they have created trusted and ongoing relationships with both old and new clients, with their tailor-made and adaptable approach they have cemented their name as a leader within the industry. This is a brilliant opportunity to join a specialist CRO, which encompasses their staff, clients and patients into their drug development process, striving to make a difference across the world.
Clinical Research Associate Role.
This position is about conducting visits to assess regulatory and protocol compliance and manage all the required documentation surrounding clinical trials. Ensuring the trials are in adherence with all protocol, SOPs, regulations and ICH-GCP. The trials will be carried out across a range of therapeutic areas; as a result, a sound knowledge of drug development is required.
Further Responsibilities Include.
If you are interested in this position, please apply now!