Clinical Research Associate (CRA)

As part of the world's leading testing, inspection and certification company, you share the benefits of our stability and growth; secure employment in a financially stable, Swiss-based company; a proud heritage that has been making the world a better, safer place for over 140 years; and a global, multicultural, and multinational organization.

Grow in a company that is the home of global knowledge and expertise; that operates in a wide range of countries, services and sectors; and that offers you endless opportunities to learn, grow and fulfill you potential!

In the spirit of continued growth, we are currently looking for a Clinical research Associate (CRA).

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.

What do you need to be successful?

• 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

• Professional: you bring quality, excellence, and ownership to everything you do
• Responsible and results-oriented: you have a sense of accountability for business results
• Committed: you bring your whole self to work with passion and focus
• Driven and eager: you are curious, flexible, and ambitious to learn from a global network
• Open to learning: from the range of different skills, backgrounds, and behaviors around you
• Capable of taking ownership and being independent
• Ambitious: you always challenge yourself to continuously improve and be the best you can be

What we can offer you:

• A truly rewarding career, working at the highest level of international standards for quality, safety and integrity
• The chance to share our growth and stability.
• Continuous learning from the best experts in the industry
• The chance to expand and enrich your career
• Professional and personal growth
• Experiences and opportunities across the global business

Do you want to be part of this?

Were you already considering a big switch in your career? Maybe this could be your next step. 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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