Clinical Reasearch Associates, CRA

Job Overview:

We are currently looking for talented Clinical Research Associates to join our team in Belgium. You would be working within our ClinOps team.

You will become a part of our team who is always ready to help. We offer a home based position so you will not spend time on unnecessary travels but at the same time we highlight a true live relationship between colleagues. You will have a possibility to devote all your professional skills and knowledge into monitoring investigational sites as we organize our work environment and responsibilities with high standards.

To join Covance in Belgium, we can only consider CRAs who are able to perform monitoring visits in French, Dutch and English

Responsibilities include: All details of site management as prescribed in the project plans Recruitment of potential investigators, preparation of EC submissions, notifications to regulatory authorities, translation of study-related documentation, organization of meetings and other tasks Negotiation of study budgets with potential investigators and cooperation with Covance legal department with statements of agreements Serious Adverse Event (SAE) reporting, production of reports, narratives and follow up of SAEs. Case Report Forms (CRF) review; query generation and resolution against established data review guidelines on Covance or client data management systems Education/Qualifications:University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure) Experience:

A minimum of 1 years of independent clinical monitoring experience, ideally at a CRO or Biopharma company, international ph I - III drug studies

To join Covance in Belgium, we can only consider CRAs who are able to perform monitoring visits in French, Dutch and English