For an international contract research association specialised in immunology, cardiovasculair and neurologic science, we are looking for a Clinical Research Associate (CRA). The organisation is a young, growing CRO with now over a 110 employees and a vast international network of experienced CRA’s. Because of the young and growing nature, it offers room for creativity for you and your co-workers to co-create, innovate and develop. Within an open culture, you can be yourself as part of a high level research organisation with a clear mission: To be the role model for and the market leader in the academic clinical research industry.
The role of CRA consists out of a broad range of tasks and responsibilities such as monitoring clinical research, feasibility checks on sites and medical ethics according to protocols, SOP’s and ICH-GCP guidelines. You will evaluate the quality and integrity of a study as well as manage the process, train researchers and maintain relationships with staff on site.
To successfully perform as a CRA you will need to be strong in communication, negotiation and ready to travel from time to time. You will be part of the CRA team, currently existing of nine Clinical Research Associates who report to the Manager Clinical Monitoring. Within the organisation it can be easy going at times, until suddenly one or two new big projects start and multiple teams have to switch gears. This asks flexibility and the ability to switch focus accordingly from you and your team.
If you are interested in this job, or in similar ones, please feel free to contact me directly.