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(Senior) Clinical Research Associate, Brussels

Covance 5/10/2018 1:07:24 PM
JOB ID: 18036 Category: Clinical Research Associate
Brussels, Belgium

   

 

Job Overview

We are currently looking for a talented Clinical Research Associates to join our Clinical Operations team in Belgium. You will have an opportunity to work on different projects for different sponsors within this department.

You will become a part of our team who is always ready to help. 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.

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

Educational background in life sciences

Experience

* Ability to monitor study sites independently according to protocol monitoring guidelines, SOPs, GCP and ICH Guidelines
* Excellent understanding of Serious Adverse Event (SAE) reporting
* Ability to resolve project-related problems and prioritize workload for self and team
* You have previous clinical research monitoring Experience (including pre-study, initiation, routine monitoring and closeout visits).

We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

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



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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 www.gettinghired.com 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).