Rising Clinical Research Associate - Site Monitoring

IQVIA LLC

Brussel Hoofdstad

Sur place

EUR 65 000 - 75 000

Plein temps

14 jours+

Générateur de candidature

Une candidature sur mesure pour ce poste — un CV personnalisé et une lettre de motivation qui correspondent directement à l’offre.

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Avantages offerts par ce poste

Company car

Mobile phone

Benefits package

Résumé du poste

IQVIA Belgium invites a Clinical Research Associate to join our Site Management team. You will monitor sites, ensure protocol adherence, and help drive data quality and regulatory compliance across studies.

We seek a university graduate with CRA experience, fluent Dutch, French, and English, and readiness to travel within Belgium. You will collaborate with study teams, manage site documents, and support start-up activities as needed.

Qualifications

University degree in scientific discipline or health care.
2+ years of experience as a CRA.
Very good computer skills including MS Office.
Excellent command of Dutch, French and English language.
Belgium based.
Organizational, time management and problem-solving skills.
Ability to establish and maintain effective working relationships; Flexibility to travel.
Driver’s license class B.

Responsabilités

Perform site monitoring visits (selection, initiation, monitoring and close-out) per scope and GCP/ICH guidance.
Collaborate with sites to drive subject recruitment and maintain regular communication.
Administer protocol and study training; manage expectations and issues.
Evaluate site practices for protocol conduct and regulatory adherence; escalate issues.
Track regulatory submissions, recruitment, CRF completion, data queries; support start-up if needed.
Maintain Trial Master File and Investigator's Site File per regulatory requirements.
Create and maintain site management documentation and visit reports.