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Brussels, BEL JOBS - Covance

Senior Associate Regulatory Submissions (Lead) Brussels, BEL

. . .th clients to support regulatory activities. Proactively interact with other Covance groups and clients to provide guidance regarding Regulatory Authority requirements and project timelines and requirements. Working with minimal supervision, it is the responsibility of the Senior Regulatory Associate to have oversight and coordination of the submission activities across the EU/Globally and to alsoRead More

Clin Res Assoc II Brussels, BEL

. . .g projects, performing remote and on-site monitoring visits. Seize the chance to be part of some of the most innovative projects of the industry! Responsibilities: * International monitoring of registry studies in Rare Disease in France, Belgium, UK and Czech Republic) for about 6 months. You will be then involved in monitoring studies in France only. * Prepare accurate and timely trip reports Read More

Project Director Brussels, BEL

. . .us European / EMEA locations. At Covance, you can redefine what is possible and discover your extraordinary potential within our Project Management Team. Our Covance Project Management team offer the unique opportunity to gain exposure across a broad clinical trial portfolio. Whether your ambition is to work at the forefront of cutting edge clinical trial design or play a pivotal role in directiRead More

Project Manager / Senior Project Manager Brussels, BEL

. . .sed or office based working, depending on location and preference. This role can be based in various European / EMEA locations. At Covance, you can redefine what is possible and discover your extraordinary potential within our Project Management Team. Our Covance Project Management team offer the unique opportunity to gain exposure across a broad clinical trial portfolio. Whether your ambition iRead More

CLINICAL TRIAL SAFETY ASSISTANT, BRUSSELS Brussels, BEL

. . .the pharmaceutical industry develop more medicines worldwide than any other company, including the top 50 best-selling drugs on the market today and * 100 % of all Oncology drugs approved in 2016. Explore this job as Clinical Safety Assistant with us and check for yourself why Covance has been named among the World´s Most Innovative Companies in Forbes´ 2017 Ranking, and more than 90% of the top Read More

Manager, Feasibility and Site Selection, home or office based EMEA Brussels, BEL

. . .gful outcomes. Responsibilities: * Accountable for supporting the development, analyses, interpretation and presentation of primary and secondary data in support of operational strategy and planning * Conducts data mining of internal and external databases and initiates/oversees the collection of primary data for use in development of robust strategies for clinical trials (country/site mix, siteRead More

CRA Site Manager Brussels, BEL

. . .on Making Skilled * Execution/Results/Process Improvement Skilled * Interpersonal skills Skilled * Ability to handle and prioritise multiple therapeutic areas and projects simultaneously * Self-starter with ability to work independently in a regional area with remote or minimal supervision * Ability to work effectively in a team/matrix environment * Ability to influence others without direct reporRead More

(Senior) Clinical Research Associate, Brussels Brussels, BEL

. . .onitoring 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 Read More

Senior Project Manager (Oncology) Brussels, BEL

. . .hips. You will collaborate with Project Managers and departments throughout Chiltern to help shape the future development of projects. Applicants must have Experience of: · Working as a Project Manager for a medium - large sized CRO · Managing full service studies · eCRF builds · Multiple vendor contracting and management · Thorough understanding of study finance and hands-on Experience of manRead More

Clin Res Assoc II Brussels, BEL

. . .t, 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 Experience Required: * Minimum of two (2) years of clRead More

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).