Sponsor‑Dedicated CRA II (Belgium) – Remote + Sign-On Bonus

IQVIA; Zaventem; À distance; EUR 42 000 - 60 000; Plein temps

Avantages offerts par ce poste

Company car

Mobile phone

Rewards package

Résumé du poste

IQVIA Belgium is seeking a motivated Clinical Research Associate II to join our sponsor-dedicated model in Belgium, home-based.

You will perform site monitoring visits per GCP/ICH, support recruitment plans, manage TMF documentation, and collaborate with cross-functional teams to ensure project success. The role requires a university degree in a scientific field and at least 18 months of on-site CRA experience, with strong Dutch, French and English communication.

Qualifications

• University degree in a scientific discipline or health care is required.
• Excellent communication in Dutch, French and English, written and spoken.
• Solid knowledge of GCP/ICH guidelines and regulatory requirements.

Responsabilités

• Perform site monitoring visits (selection, initiation, monitoring and close‑out) per scope and GCP/ICH.
• Drive subject recruitment plans with sites to improve predictability.
• Administer protocol training to sites and maintain open communication lines.
• Evaluate site practices for protocol conduct and regulatory adherence; escalate issues.
• Track regulatory submissions, recruitment, CRF completion, data queries and resolution.
• Ensure TMF/ISF documents are filed and maintained per requirements.
• Create, consolidate and submit visit reports and follow-up letters.
• Collaborate with study team members to support project execution.

Connaissances

Dutch

French

English

GCP knowledge

ICH guidelines

Communication

Interpersonal skills

Problem solving

Cross-cultural

Collaboration

Formation

University degree in scientific discipline or health care

Description du poste

IQVIA Belgium is seeking a motivated Clinical Research Associate II to join our sponsor-dedicated model in Belgium, home-based.

You will perform site monitoring visits per GCP/ICH, support recruitment plans, manage TMF documentation, and collaborate with cross-functional teams to ensure project success. The role requires a university degree in a scientific field and at least 18 months of on-site CRA experience, with strong Dutch, French and English communication.