Biomarker Project Lead — Clinical Trials & GLP Compliance

Eurofins; Breda; On-site; EUR 70,000 - 100,000; Full time

Job summary

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.

Qualifications

• 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.

Responsibilities

• 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.

Skills

Bioanalytical skills

Customer focus

Communication skills

Interpersonal skills

Relationship management

Flexible work ethic

Education

Master’s degree in Biochemistry/Life Sciences

Bachelor degree in Biochemistry/Life sciences with significant industry experience

Job description

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.