Clinical Data Assistant (BB-60AF0)

Trouvé dans: Neuvoo Bulk BE


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 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.

At our Clinical Pharmacology Unit, located at Stuivenberg Hospital Antwerp, we are currently looking for a Clinical Data Assistant.

Job description

As a Clinical Data Assistant, you will be responsible for the planning and execution of the eSource design testing. You will work together with the different study teams to ensure the most efficient design is applied for all involved parties. At the same time, you will ensure that the designs are properly validated before the first use.

As a Clinical Data Assistant, you will also be involved in the review of the study specific training instructions linked to the eSource system to ensure the training is a 100% match with the systems expectations during trial conduct.

1. Testing and Validation of eSource study design

  • All dynamic fields work as expected
  • Edit checks fire as expected
  • All expected items are available
  • All standard processes are included
  • 2. Review study specific instructions

  • Ensure completeness (each available data point is described)
  • Ensure specifics are described 
  • Ensure content reflects the actual eSource study design
  • 3. Create / Review eSource Specific manuals

  • As tester of the study design you will review / create the general instruction manuals for the floor staff.
  • Searched Profile

    What do you need to be successful?

  • Strong organisational skills
  • Strong communication skills, flexible, quality minded and stress resistant
  • Team player, focused on problem solving
  • Fluent in Dutch and English (written and oral)
  • Strong computer skills
  • We offer

    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 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.

    calendar_todayil y a 1 jour

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