Coördinator SAS Programmers

Company Description

At SGS, you can choose!

First of all, out of our various vacancies. However, SGS also gives you another choice.
Do you choose to expand or to enrich? We are not only looking for colleagues who can go in to depths of their discipline. We are equally as much looking for colleagues who we call ‘connectors’, people who can connect our diversity to our services. To each other. And this way, enrich our business.

SGS is the world’s leading inspection, verification, testing and certification company. We’re also the benchmark worldwide for quality and integrity. And that makes us very proud. This can only happen thanks to almost 100 000 colleagues worldwide, with more than 1650 employees in Belgium only. Our employees give 110% of themselves every day, divided over all expertises, branches and cultures. Our coworkers build their own way inside the company, the services and the expertise.

SGS Life Sciences carries out all type of services for pharmaceutical and biotechnology companies, from coordination and running of clinical trials with new molecules or techniques on human beings, to support and consultancy on post marketing registration activities.
SGS Life Sciences has also expertise in the quality control of pharmaceuticals.

We are currently looking for a Coördinator Secure Data Office Programming

Job Description

The main responsibility of the Secure Data Office Programming Coordinator (SDOPC) consists of performing programming activities on clinical trials but more focused on coordination and planning of these activities, overseeing the Secure Data (SD) Office processes and coaching of junior SDOPs (Secure Data Office Programmers) in the SD Office team.

Main tasks of the SDOPs are:
· Program and validate new SAS macros
· Program and validate NCA and NONMEM datasets
· Creation of randomisation lists specifications, randomisation lists and medication kit lists

You act as the right hand of the Executive Manager Secure Data Office for the overall management and planning of all SDOP tasks on the clinical trials processed in the SD Office team.
You work closely together with the SD Office Team Managers (Team Manager Secure Data Office and Team Manager Secure Data Management) in the SD Office team with respect to planning, knowledge sharing and general programming or process improvement initiatives.

Qualifications

· Master’s degree in Statistics
· In depth knowledge of SAS programming language
· At least 2 years SAS programming experience within the clinical research field
· Fluent and proficient knowledge of English
· Good communication skills
· Positive, constructive, professional attitude towards colleagues and sponsors
· Coaching and people management skills
· Flexible
· Well organized
· Time management skills
· Quality minded
· Accurate
· Problem solving mind
· Proactive
· Stress resistant

You will report to the Executive Manager Secure Data Office.

Additional Information

What we have to offer:

You will receive an extensive training where necessary
We work towards your professional growth and will support you during your career development path
A good work-life balance

Do you want to be part of this?

We are looking forward to hearing from you!

Send us your story and your resume via the apply button and maybe you will soon join us for work and coffee breaks.

Still have questions? Heidi Aerts can give you more details about the job.
Send her an e-mail at [email protected]