Biomarker Project Lead — Clinical Trials & GLP Compliance

Eurofins

Breda

Vor Ort

EUR 70.000 - 100.000

Vollzeit

14 Tage+

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Zusammenfassung

Eurofins Central Laboratory in Breda, Netherlands, seeks an Analytical Project Manager to oversee biomarker studies within clinical trials, ensuring GMP/GCP compliance and client satisfaction.

You will define milestones, manage budgets, coordinate with sponsors and audits, and sustain strong internal and external relationships through clear communication and a proactive, energetic approach.

Qualifikationen

  • Master’s degree in Biochemistry/Life Sciences or Bachelor degree with significant industry experience.
  • GxP/GLP regulatory experience.
  • Biomarker experience in CRO or pharmaceutical settings.
  • Strong customer focus and communication abilities.

Aufgaben

  • Manage biomarker studies in clinical trials according to regulatory requirements.
  • Provide operational input into quotes/proposals to align capabilities with client needs.
  • Define project milestones and monitor performance from contract to invoice.
  • Ensure studies adhere to global standards and budget responsibilities.
  • Complete study files for regulatory inspections and support sponsor/audit activities.

Kenntnisse

Bioanalytical skills
Customer focus
Communication skills
Interpersonal skills
Relationship management
Flexible work ethic

Ausbildung

Master’s degree in Biochemistry/Life Sciences
Bachelor degree in Biochemistry/Life sciences with significant industry experience

Jobbeschreibung

Eurofins Central Laboratory in Breda, Netherlands, seeks an Analytical Project Manager to oversee biomarker studies within clinical trials, ensuring GMP/GCP compliance and client satisfaction.

You will define milestones, manage budgets, coordinate with sponsors and audits, and sustain strong internal and external relationships through clear communication and a proactive, energetic approach.

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