Belgium CRA: Drive Clinical Trial Excellence

BioSpace

Namen

Sur place

EUR 60 000 - 80 000

Plein temps

Il y a 4 jours
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Résumé du poste

AbbVie is seeking a Clinical Research Associate (CRA) to support clinical studies in Belgium. You will partner with investigators and site teams to promote study delivery, data quality, and compliance. You will monitor sites, ensure patient safety, and help recruit and retain participants, while maintaining audit readiness.

You will collaborate with the Central Monitoring team and contribute to training and mentoring of junior CRAs, ensuring high-quality data and site performance across studies.

Qualifications

  • Degree in health-related discipline (e.g., Medicine, Life Sciences, Nursing).
  • At least 1 year of clinically related experience, incl. 6+ months in monitoring.
  • Familiar with risk-based monitoring, on-site and remote.
  • Fluency in French, Dutch and English is required.

Responsabilités

  • Serve as the primary contact for assigned investigative sites and coordinate with stakeholders.
  • Conduct site evaluation, initiation, monitoring, and close-out per protocol and quality standards.
  • Support patient safety and data quality throughout the trial.
  • Mentor and train less experienced CRAs and contribute to site engagement strategies.

Connaissances

Clinical monitoring
Regulatory knowledge
GCP/ICH familiarity
Multilingual: EN/FR/NL

Formation

Health-related degree

Description du poste

AbbVie is seeking a Clinical Research Associate (CRA) to support clinical studies in Belgium. You will partner with investigators and site teams to promote study delivery, data quality, and compliance. You will monitor sites, ensure patient safety, and help recruit and retain participants, while maintaining audit readiness.

You will collaborate with the Central Monitoring team and contribute to training and mentoring of junior CRAs, ensuring high-quality data and site performance across studies.

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