Senior Start-Up & Regulatory Specialist (Remote, Belgium)

IQVIA LLC

Zaventem

À distance

EUR 55 000 - 75 000

Plein temps

14 jours+

Générateur de candidature

Une candidature complète en une minute — CV personnalisé et lettre de motivation, prêts à envoyer.

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Avantages offerts par ce poste

Home-based flexibility

International exposure

Résumé du poste

IQVIA is seeking a Senior Associate RSU Specialist in Belgium (home-based). The role focuses on site activation, regulatory submissions, and contract negotiations, requiring 3.5–5 years of clinical research experience and fluency in Dutch and/or French with strong English communication.

You will collaborate with Site Activation Managers and project teams to ensure compliant, timely study start-up and activation across Belgian and international regulations, leveraging solid planning and

Qualifications

Bachelor's Degree in Life Sciences or related field.
Approximately 3.5–5 years of experience in clinical research.

Responsabilités

Serve as the primary point of contact for investigative sites and project teams.
Coordinate country-specific site activation and regulatory activities.
Prepare, review, and distribute regulatory documentation for completeness and compliance.
Track and manage regulatory submissions, ethics committee submissions, and CTAs.
Support contract negotiations and timelines.
Maintain records in internal systems and tracking tools.
Monitor milestones and identify risks with mitigation plans.
Provide local regulatory expertise to project teams.
Perform quality reviews of site documentation.
Collaborate with sponsors and cross-functional teams for study start-up.