Job 1000 van 1000

Plaats

Bruxelles
België
België

Contract

Vooltijds, Onbepaalde duur

Datum gepubliceerd

2026-05-20

Online to:

2026-07-19
EUR 20.00 HOUR

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Clinical Research Associate

Hlx Life Sciences
België
Andere
1 week geleden

Managing and monitoring clinical trial sites to ensure studies are conducted according to protocol, regulatory requirements, and Good Clinical Practice (GCP) standards. Precision is a mid-sized CRO known for its strong specialization in oncology, rare diseases, and precision medicine trials.

Job Responsibilities

Monitor clinical trial sites remotely and onsite
Ensure patient safety and data integrity
Review source documentation and case report forms (CRFs)
Support site start-up activities, ethics submissions, and regulatory documentation
Train and support investigators and site staff
Track study progress and maintain trial management systems
Prepare sites for audits and inspections
Identify and resolve protocol deviations or compliance issues

Please apply and attached your CV as the role is for an ASAP start!!

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