Clinical Research Associate II - Belgium (EU)

IQVIA; Zaventem; Sur place; EUR 55 000 - 75 000; Plein temps

Résumé du poste

IQVIA Biotech in Belgium is seeking an experienced Clinical Research Associate to participate in Phase I–IV trials and monitor sites in compliance with GCP. You will perform site evaluations, initiation visits, and ongoing monitoring, coordinating with the CTM/Lead CRA to ensure protocol adherence and data integrity.

Fluency in Dutch and English is required (French a plus). Minimum 1–2 years of onsite monitoring experience is expected, with ability to work independently in a matrix team and

Qualifications

• Minimum of 1–2 years of onsite monitoring experience.
• Strong knowledge of the clinical research process.
• Excellent written and verbal communication skills.
• Ability to work independently within a matrix team.
• Knowledge of GCP/ICH guidelines.
• Dutch and English language skills; French a plus.

Responsabilités

• Participates in investigator recruitment and site evaluation visits.
• Prepares for initiation, reviews protocol and regulatory issues.
• Assists in resolving site file audits and issues.
• Ensures adherence to Good Clinical Practices during on-site visits.
• Documents accountability and storage of trial materials.
• Reviews data quality via in-house and source verification.
• Serves as primary contact between IQVIA Biotech and investigators.
• Attends investigator meetings and study-related meetings.
• Ensures study deliverables meet timelines.
• Mentors junior CRAs and new staff.

Connaissances

Clinical research

GCP/ICH

Onsite monitoring

Dutch & English

Description du poste

IQVIA Biotech in Belgium is seeking an experienced Clinical Research Associate to participate in Phase I–IV trials and monitor sites in compliance with GCP. You will perform site evaluations, initiation visits, and ongoing monitoring, coordinating with the CTM/Lead CRA to ensure protocol adherence and data integrity.

Fluency in Dutch and English is required (French a plus). Minimum 1–2 years of onsite monitoring experience is expected, with ability to work independently in a matrix team and