Sr. Clinical Research Associate

📋 Description

• Manage full clinical site monitoring for multiple projects.
• Lead CRA activities and mentor CRAs.
• Act as primary liaison between CRAs and study teams.
• Oversee site recruitment, data/doc management and training.
• Ensure SOPs, GCP compliance and regulatory filings.
• Collaborate with stakeholders across multinational studies.

🎯 Requirements

• College diploma/degree; 4–6 years of related experience.
• Self-motivated with strong communication skills.
• Attention to detail; collaborative.
• Critical thinking abilities.
• Ability to regularly travel to sites.
• Fluent in English, Dutch and French.

🎁 Benefits

• Sign-on bonus of €3,000.
• Annual bonus target of 8% of salary.
• Monthly stipend for internet/communications (€157.83).
• Monthly cell phone stipend (€40).
• One-time expense reimbursement up to €500.
• Mileage reimbursement for travel.