To us it’s personal.

(Senior) Clinical Research Associate in Belgium

Covance 1/25/2019 1:51:14 PM
JOB ID: 27550 Category: Clinical Research Associates
Brussels, Belgium



Job Overview

We are currently looking for a talented Clinical Research Associates to join Covance in Belgium! This is a Sponsor dedicated position which will give you the opportunity to work with and for one of the most innovative pharmaceutical company in the industry.

You will be part of a great and dynamic team, with the possibility to devote all your professional skills and knowledge into monitoring investigational sites as we organize our work environment and responsibilities with high standards.

Location: Brussels / Home-Based possible with presence required in client offices on a regular basis

This is time to join our EMEA FSPx Team!

Education / Qualifications

* University/college degree (life science preferred), or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology)
* In lieu of the above requirement, candidates with three (3) or more years of relevant clinical research Experience in pharmaceutical or CRO industries may be considered
* Thorough knowledge of ICH Guidelines and GCP including a basic understanding of regulatory requirements
* Thorough knowledge of monitoring procedures
* Basic understanding of the clinical trial process

- * Ability to monitor study sites independently according to protocol monitoring guidelines, SOPs, GCP and ICH Guidelines
* Have a full understanding of the Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs
* Good planning, organization and problem solving abilities
* Ability to work with minimal supervision
* Good communication and interpersonal skills
* Good analytical and negotiation skills
* Computer competency
* Fluent in local office language and in English, both written and verbal
* Works efficiently and effectively in a matrix environment
* Minimum of two (2) years of clinical research monitoring Experience (including pre-study, initiation, routine monitoring and closeout visits)

Apply now and join us!

Key words:

Clinical Research, CRA II, Clinical Research Associate, Belgium, Monitor, Monitoring, Senior Clinical Research Associate, CRA I, Field Based, CRO, Pharmaceutical, CRA

Position Type: Full-Time

Location: Brussels, BEL - Belgium


Covance Recruiting Process

Below is a general Overview of Our Recruiting Process

If you’d like to work for us, please submit your resume/CV online. If your ability to use or access our electronic application is limited due to a disability, please visit or call 1-800-978-4473 for help.

We consider applications from everyone who is interested in a position with us and who meets the required criteria and qualifications.

If your application is selected, someone from our recruiting team will contact you to arrange an initial screen. We may carry this out over the phone or at a face-to-face meeting. You must complete the screen to be considered for the position.

Based on the results of the initial screen, we may invite you to an interview. One of our recruiting team members will contact you to arrange this. The process may involve several interviews, initially over the phone, and then face-to-face with different members of the hiring team.

Our interviews follow a behavioral-based format. This means we’ll ask you to give us information that’s specific to your professional and educational experiences.

Hiring team members will share and discuss their input and then make their decision.

If you’re the person who best meets the requirements of the position, a member of the hiring team will get in touch to make you an offer of employment. Covance is an eVerify employer (United States only).