e-CRF Designer in Mechelen

Beschrijving

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 95 000 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 Science Services 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 Science Services has also expertise in the quality control of pharmaceuticals. We are currently looking for an e-CRF Designer – Master in Sciences (Mechelen) The main tasks of the (e-)CRF Designer ((e-)CRF-D) consist of designing data collection tools (DCT) (e-CRFs or paper CRFs) based on a clinical trial protocol and the sponsor’s requirements and specifications. The (e-)CRF-D is also responsible for the thorough follow-up of the data collection tool. Your day to day tasks:  Generate an (e-)CRF based on the clinical trial protocol and/or predefined specifications Ensure review of the (e-)CRF by other parties (internal and external) until finalization Incorporate relevant comments in the (e-)CRF Implement changes to the (e-)CRF when needed Generate and maintain the eDC tool Data Validation Rules based on the DVR specifications Review the proof copy of the printer company in case of a paper CRF 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 and Dutch is very good, in 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:  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 a salary package adapted to your needs (incl. retirement plan, meal vouchers, …) Do you want to be part of th...

Extra informatie

Status

Open

Opleidingsniveaus

HBO5

Plaats

Mechelen

Dienstverbanden

Fulltime (startersfunctie)

Gepubliceerd op

06-12-2024

Beroepsgroepen subcategorie

Administratief

Rijbewijs nodig?

Nee

Auto nodig?

Nee

Motivatiebrief verplicht?

Nee

Talen

Arabisch