Clinical Quality Risk Manager for Trials & Inspections

Johnson & Johnson Co.

Beerse

Sur place

EUR 80 000 - 138 000

Plein temps

Il y a 4 jours
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Résumé du poste

Johnson & Johnson is seeking a Manager, Quality Clinical Risk Management to join the R&D Quality CRM team. This role leads clinical risk management across trials and programs, translating risk signals into proactive mitigation and quality decisions.

It combines hands-on risk ownership with cross-functional influence and inspection readiness. The position requires 8+ years in healthcare quality, BA/BSc or equivalent, and strong proficiency in quality systems, CAPA, and regulatory expectations

Qualifications

  • Proficiency in Microsoft Office Applications.
  • Excellent written and verbal English skills.
  • Strong interpersonal and communication abilities.
  • Proven quality management experience in healthcare/pharma.
  • Experience working in cross-functional teams and with external partners.

Responsabilités

  • Identify and assess key clinical risk in trials and programs.
  • Lead risk monitoring reviews and drive mitigation actions.
  • Prepare and maintain quality risk plans and CAPA strategies.
  • Provide guidance on investigation, escalation, and reporting to health authorities.
  • Support inspection readiness and sponsor-monitor interactions.
  • Coach team members on risk monitoring and quality practices.

Connaissances

Microsoft Office
English language
Interpersonal skills
Quality management
Cross-functional collaboration

Formation

BA/BSc or equivalent

Outils

Tableau
Spotfire

Description du poste

Johnson & Johnson is seeking a Manager, Quality Clinical Risk Management to join the R&D Quality CRM team. This role leads clinical risk management across trials and programs, translating risk signals into proactive mitigation and quality decisions.

It combines hands-on risk ownership with cross-functional influence and inspection readiness. The position requires 8+ years in healthcare quality, BA/BSc or equivalent, and strong proficiency in quality systems, CAPA, and regulatory expectations

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