Are you a CRA less than 1 year of monitoring experience OR a research nurse or study coordinator with an oncology background that is looking to use your skills in a whole new way? If so, it's your time to SHINE at Covance!
We have helped the pharmaceutical industry develop:
Now is your time to become an integral part of these achievements. If you are an experienced nurse or study coordinator with an oncology background that wants to pursue a career as a Clinical Research Associate/ CRA…we will TRAIN you!
at our Covance Monitoring Excellence Academy.
Explore this CRA I job with us and check for yourself why Covance is known to promote 2.5x more employees annually than the average company in the biopharmaceutical sector.
Our sponsor-dedicated team is rapidly growing in Brussels. We have an office based, permanent Clinical Research Associate I job available to work directly with one of our main clients.
This is an international job environment: this is why we need you to be fluent (both speaking & writing) in English, French and Dutch.
As our CRA I you will conduct site monitoring responsibilities for Clinical trials, according to Covance Standard Operating Procedures, ICH guidelines and GCP, including Pre-study, Site Initiation, Routine Monitoring, and Close-out Visits (as per the training status of the CRA I-MEA program).
You will participate, conduct or assist with the following duties as consistent with training completed:
Please note that in order to be admitted in this highly sought after CRA development initiative, we need you to bring a minimum of some months experience as a CRA, or a minimum of 1 year experience in a related role, such as:
Preferred: background in oncology