Clinical Research Associate – Site Monitoring & Growth

IQVIA LLC; Zaventem; Vor Ort; EUR 50.000 - 65.000; Vollzeit

Benefits dieser Stelle

Company car

Mobile phone

Benefits package

Zusammenfassung

IQVIA Belgium is seeking a Clinical Research Associate to support monitoring visits, recruitment plans, and regulatory compliance across multiple therapeutic areas. You will work in a Belgium-based role with travel flexibility and contribute to delivering high-quality clinical research services.

The position requires a university degree in a scientific discipline or health care, plus experience in pharma or clinical trials, and fluency in Dutch, French, and English.

Qualifikationen

• University degree in scientific discipline or healthcare.
• Experience in Pharma industry or clinical trials.
• Excellent computer skills including MS Office.
• Fluency in Dutch, French and English.

Aufgaben

• Performing site selection, initiation, monitoring and close-out visits.
• Supporting the development of a subject recruitment plan.
• Evaluating site practices for regulatory compliance (GCP/ICH).
• Managing progress by tracking regulatory submissions, recruitment, CRF completion, data queries.
• Collaborating with study-site experts and client representatives.

Kenntnisse

Dutch language

French language

English language

Organizational skills

MS Office

Ausbildung

University degree in science/healthcare

Tools

MS Office

Jobbeschreibung

IQVIA Belgium is seeking a Clinical Research Associate to support monitoring visits, recruitment plans, and regulatory compliance across multiple therapeutic areas. You will work in a Belgium-based role with travel flexibility and contribute to delivering high-quality clinical research services.

The position requires a university degree in a scientific discipline or health care, plus experience in pharma or clinical trials, and fluency in Dutch, French, and English.