Clinical Research Associate (CRA)

☞ SGS

看过: 225

更新日: 26-11-2025

位置: Mechelen Antwerp

类别: R & D

行业: Oil Gas Retail Office Equipment Consumer Services

水平: Associate

工作类型: Full-time

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工作内容

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.

SGSis 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 looking for a Clinical Research Associate (CRA).

Job Description

As a clinical research associate you will be responsible for:
  • Participating in the trial set up activities
  • Preparing, translating, reviewing, finalizing, tracking and filing study documents
  • Conducting site initiation visits, monitoring visits (on-site and remote, in accordance with the monitoring plan) and close-out visits at assigned clinical site(s) according to applicable regulations, SGS procedures and study specific documents.
  • Writing site visit reports
  • Verifying the IMP management process at site (storage, return, accountability…)
  • Managing trial sites
  • Overseeing overall integrity of the study, ensuring the rights and well-being of human subjects are protected and are in accordance with protocol
  • Ensuring compliance of the trial conduct with the protocol and the applicable guidelines, regulations and SGS procedures
You will work in close collaboration with other CRAs and the Study Team to ensure that quality and milestones are achieved within the budget and you will maintain regular contacts with the sponsor, project team and investigator.

Qualifications
  • You have obtained a university degree (equal to 4 years of college) in (para-) medical, pharmaceutical, sciences, life-sciences or bio-sciences. An equally recognized degree and/or relevant qualifications by experience may also be acceptable and will be evaluated on a case-by-case basis.
  • You can work in a self-driven capacity, with a sense of urgency and limited need for oversight
  • You are fluent in both Dutch and English; knowledge of French is an asset
  • You are a strong communicator and have strong organisational skills
  • You work well independently as well as in a team
  • You are constantly dotting the i's and crossing the t's
  • you have a good knowledge of ICH GCP and European Directives 2001
  • You are accountable, helpful, dedicated and flexible
  • You are willing to travel, if necessary
Additional Information

Whatwehave 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. Still have questions? Anneleen can give you more details about the job. Send her an e-mail at anneleen.vanbuggenhout@sgs.com
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最后期限: 10-01-2026

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