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Mechelen, BEL JOBS - Covance

Lead RAVE Study Builder Mechelen, BEL

. . . Study Builder within our Early Phase (Phases I & II) data management department. The Lead RACE Study Builder will provide technical services for building clinical trial databases within EDC environments (mainly RAVE) for assigned clinical trial projects to achieve project integrity, on time delivery and quality data. Working within our early phase group we offer, in a word, variety… In the typeRead More

Clinical Data Manager Mechelen, BEL

. . . 1. Create protocol folder(s) for study documentation 2. Add entries into individual protocol spreadsheet 3. Review Statement of Work (SOW) for study scope 4. Ensure start-up packet delivery to clients 5. Contact clients for initial study discussion and determine authors of Data Transfer Specifications (DTS) 6. Provide recommendations and alternatives to optimize data quality 7. Collaborate with Read More

Regional Study Coordinator - Associate project manager Mechelen, BEL

. . .liaison and communication between the Global Study Management and all the various departments involved in the study. We are offering a permanent or 2 year contract (renewable), based in our Mechelen or Brussels (Belgium) location or remotely. About the Job Within this position, your duties will include: * Act as regional liaison between Global Study Manager and various CLS departments involvedRead More

Study Design Lead - Technical Project Management Mechelen, BEL

. . .of Work document (key client deliverable) and should demonstrate leadership across the Covance study team, keeping a collaborative attitude and fostering excellent communication within the team, demonstrate agility to deal with conflicting priorities and possess appropriate self-management skills. We are offering either a permanent or 2 year contract (renewable), full time position, based in our Read More

Global Study Manager - Project Manager Mechelen, BEL

. . .s, or remotely in Belgium for a permanent or 2 years contract opportunity (renewable). About the Job As a key member of the Project Management department, you will be managing a portfolio of global, high complexity clinical studies. As such, your main responsibilities will entail: * Being the key contact between the clients, the various departments within our Central Laboratory organization, otRead More

Clinical Data Manager Mechelen, BEL

. . . 1. Create protocol folder(s) for study documentation 2. Add entries into individual protocol spreadsheet 3. Review Statement of Work (SOW) for study scope 4. Ensure start-up packet delivery to clients 5. Contact clients for initial study discussion and determine authors of Data Transfer Specifications (DTS) 6. Provide recommendations and alternatives to optimize data quality 7. Collaborate with Read More

Study Design Lead / Technical Project Management - 2 year contract Mechelen, BEL

. . .tely in Belgium for a 2 years contract opportunity. About the Job As a key member of the Project Management department, you will be responsible for the design of the Covance Statement of Work (SOW). From this essential document, which is a reflection of the Study Protocol provided by our clients, derive all the services provided by Covance Central Laboratories throughout the course of a clinical Read More

Data Project Manager - I Mechelen, BEL

. . .mpletion activities. * Develop [Global] Data Management Plans and Quality Management (QM) Plans that will deliver accurate, timely, consistent, and quality clinical data. * Identify and implement solutions to project data management issues and concerns, including proactive prevention strategies based on metrics and forecasts. * Serve as the project and client liaison including management and proviRead More

Principal Statistical Programmer Mechelen, BEL

. . .using the SAS programming language * Candidates must be fluent in English language (both verbal and written) Join our growing team and discover your extraordinary potential by working as a Covance Principal Statistical Programmer. As a Principal Statistical Programmer at Covance you will be responsible for all statistical programming deliverables of one or more complex clinical trials. You will wRead 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).