Senior CRA (MedTech) – Global Trials & Impact

Arcadis; Machelen; Sur place; EUR 65 000 - 100 000; Plein temps

Avantages offerts par ce poste

Competitive compensation

Global project teams

Professional development

Flexible environment

Résumé du poste

Arcadis is seeking an experienced Senior Clinical Research Associate to support and monitor clinical studies within a MedTech environment. You will manage multiple study sites, ensure protocol and GCP compliance, and drive data quality and study performance.

Applicants should have 4+ years of site monitoring experience, strong communication skills, and willingness to travel up to 80% of the time. English fluency is required, with a scientific background preferred.

Qualifications

• Bachelor's or Master's degree in Life Sciences, Biological Sciences, Nursing, Pharmacy, Biomedical Sciences, or related field.
• Minimum of 4 years of recent site monitoring experience as a Clinical Research Associate.
• Experience in clinical research is required.
• GCP knowledge and regulatory understanding are essential.

Responsabilités

• Manage and oversee multiple clinical study sites across one or more clinical projects.
• Conduct site initiation, routine monitoring, and close-out visits.
• Ensure the safety, rights, and well-being of study participants at assigned sites.
• Monitor compliance with study protocols, GCP, and regulatory requirements.
• Review and verify clinical data for accuracy, completeness, and quality.
• Support patient recruitment and retention at study sites.
• Identify, elevate, and help resolve study-related issues and CAPAs when required.
• Maintain ISF and essential study documentation.

Connaissances

Site monitoring

English fluency

Stakeholder management

Organizational skills

Travel readiness

Formation

BSc/MSc Life Sciences

Outils

MS Office

Description du poste

Arcadis is seeking an experienced Senior Clinical Research Associate to support and monitor clinical studies within a MedTech environment. You will manage multiple study sites, ensure protocol and GCP compliance, and drive data quality and study performance.

Applicants should have 4+ years of site monitoring experience, strong communication skills, and willingness to travel up to 80% of the time. English fluency is required, with a scientific background preferred.