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Brussels, BEL JOBS - Covance

CRA Asst Brussels, BEL

. . .m CRF review, query generation and resolution against established data review guidelines, under direct supervision on Covance or client data management systems, as assigned by management. Other duties/responsibilities include: - Assist with generation and reconciliation of queries to investigative sites/clients to resolve problem data. - Assist with the management of study supplies and organizRead More

Clinical Team Lead Brussels, BEL

. . .n / Qualifications * Educated to degree level in a science or medical speciality. A post graduate qualification is highly desirable. * Knowledge of clinical trial design and development in relevant therapeutic areas. * Thorough working knowledge of all aspects of GCP and the regulatory/ethical framework * Ability to plan, set and manage clinical trial budgets * Good IT skills in, e.g. MS Office, Read More

Senior CRA Belgium Brussels, BEL

. . .nsultant providing your expertise to the sponsor. Your responsibilities, besides monitoring will also involve: o EC submissions management o Contract set up with the sites and any provider when needed Successful candidates will be fluent in French, English and Flemmish and will enjoy the benefits of working for a company that values a WORK / LIFE BALANCE. This is time to join our EMEA FSPxTeaRead More

Sr Clin Proj Admin Brussels, BEL

. . .nd office-based position at our Client's office in Belgium. Responsibilities: - Provide support to the Projects Managers (Billing follow up, proofreading and editing correspondence, large and small documents, mailings, shipment of study files, fax and photocopy documents, assemble study documents, and arrange meetings, etc.) - Provide support with Contracts - Set up and maintain clinical inveRead More

Clinical Team Lead Brussels, BEL

. . .ole is essential. Primary duties: * Responsible and accountable for the management of the clinical study team with particular emphasis on teamwork, quality, timelines, budget, metrics and compliance with the project plans and SOPs. * Develop the strategy, plans, tools and training to oversee and assess performance of the clinical team, in the conduct and compliance of site visits (on site and reRead More

Project Manager, OES Brussels, BEL

. . .ing project teams, communications, risk, scope, schedule, cost, quality, and stakeholders, effectively ensuring that variance from plan is proactively and effectively mitigated and client expectations are met. The Senior Project Manager is expected to have a working knowledge of drug development and clinical study execution in the Interventional Post Market and Observational study arena. They alsoRead More

Medical Writer II-CDS Brussels, BEL

. . .on level documents under guidance of senior staff. * Production of scientific publications and other documents (e.g., abstracts, posters, manuscripts, etc.). * Interpretation of clinical, pharmacokinetic, pharmacodynamic and statistical results as appropriate. * Lead and coordinates activities of other writers on higher complexity narrative projects. * Ensure timely delivery of high quality documeRead More

Senior CRA - Home-based in Belgium Brussels, BEL

. . .us Pharmaceutical company. * Unlike some CRA roles you will not be pushed to satisfy unrealistic ‘monthly visit' targets * The job is permanent and full time * Your Line Manager will be based in France, possibly in your region * You will be joining a big team with a well organised structure and robust processes in place As an Experience d Sr.CRA you'll be involved in initiation, routine & close oRead More

Statistical Programmer II Brussels, BEL

. . .y potential by working as a Covance Statistical Programmer II within our Early Phase (Phases I & II) statistical programming department. As a Level II Statistical Programmer at Covance you will be responsible for providing SAS programming support in terms of SDTM and ADaM datasets and tables, figures and listings (TFLs) for reports. You will also assume the role of Lead Programmer for allocated stRead More


. . .oject Management organization is strong in Europe: 200+ PMs. The Covance´s Oncology PM team offers unique opportunities to gain exposure across a broad clinical trial portfolio. Whether your ambition is to work at the forefront of innovative clinical trial design or play a pivotal role in leading and coordinating global clinical trials in Big Pharma, we have the right job for you. WHAT MAKES THISRead 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 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).