수평: Entry level

직업 종류: Full-time

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작업 내용

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 more than 90 000 colleagues worldwide, with 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 Sciencescarries 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 Scienceshas also expertise in the quality control of pharmaceuticals.

In the spirit of continued growth and to help improve our business, we are currently seeking for a Master or PhD (biomedical) sciences with hands-on computer skills.

Job Description

Every clinical trial needs its own application in order to collect all the data. Our EDC-team, which stands for Electronic Data Capturing, is the team within SGS, that is responsible for designing, configuring and validating these applications.

You, as a e-CRF designer, will play a very important role in designing the data collection applications based on a clinical trial protocol and the pharma/biotech requirements. For this, you will receive extensive training during which you can enrich your scientific know-how with a flavor of computer programming.

You will also be responsible for the thorough follow-up of the data collection application. This means that you will ensure the review of the applications by working closely together with our pharma/biotech partners. You will incorporate relevant comments and implement changes when needed. Lastly, you will also configure/program the data validations rules based on the specifications.

Qualifications

What do you need to be successful?
  • You have obtained a master’s degree in a paramedical area or biomedical sciences. A first experience in clinical research on your track record is a big plus, but not obligatory.
  • Your knowledge of English is very good, in both written as well as spoken.
  • You are PC-minded!
  • You are eager to learn.
  • You’re a curious personality with a great eye for detail and quality minded.
  • You are easy with words and possess excellent communications skills.
  • You have a positive, constructive, professional attitude.
  • You are stress-resistant, and you enjoy solving problems.
  • You are able to set priorities and meet deadlines.
  • What’s a team without a team player?
  • You love to work in team and can handle stress like a pro, thanks to your well-organized competences.
What We Have To Offer

Additional Information

Were you already considering a big switch in your career? Maybe this could be your next step. At SGS you can count on an interesting position where you can take responsibility. Come enjoy our fun team of colleagues and on top of that, we will reward you with an interesting salary package (incl. retirement plan, meal vouchers, …)

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? Anneleen Vanbuggenhout can give you more details about the job. Send her an e-mail at anneleen.vanbuggenhout@sgs.com
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마감 시간: 31-12-2025

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