Archer is a young, dynamic and growing Contract Research Organization (CRO) based in Bioville, Diepenbeek, Belgium. We are specialized in providing full support for clinical studies with medical devices in Europe.
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Archer Research is looking for a well-motivated CTA to support the team in the day-to-day administrative activities. You will have the opportunity to be involved in this constantly growing and inspiring international environment.
Who are we looking for?
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You have experience as a Clinical Trial Assistant or Medical Management Assistant.
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You have a curiosity for clinical research & medical innovations.
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You love to make meaningful contributions.
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You are familiar with guidelines like Good Clinical Practice (GCP) and ISO14155.
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You have a Bachelor or Master’s degree in one of the Life Sciences, or Medical Management Assistant.
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You love to build strong relationships with site staff.
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You have excellent written and verbal communication skills including good command of Dutch and English. Knowledge of German and/or French is a plus.
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You have the ability to work predominately in our offices with the flexibility to work remotely from home.
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People describe you as being confident, flexible, pro-active and result-driven, with attention to detail and accuracy in work.
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You excel in effective time management and organization, with the ability to manage multiple priorities across various clinical studies within various disciplines and with a problem-solving mentality.
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Computer skills, including working knowledge of Microsoft Word, Excel, PowerPoint are checked in your competences list. Knowledge of Electronic Data Capture (EDC) systems is a plus.
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What is your role?
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Support the Archer Research study teams with efficient document management to assure smooth and reliable administration and follow-up on the clinical studies.
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You assist the clinical team in the preparation, handling, distribution, filing, and archiving of clinical documentation, reports and correspondence, as well as creation and periodic review of study files (eTMF, eISF) for completeness.
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You accurately update and maintain clinical systems/logs that track site compliance and performance.
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You act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.
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You also have the opportunity to be involved in quality assurance administration of this growing company, together with the Quality Manager.
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Interested to join the Archer Research team?
Do not hesitate to send your CV to info@archerresearch.eu.
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