Remote Senior Site Activation Specialist – Belgium

IQVIA LLC

Henegouwen

À distance

EUR 83 000 - 117 000

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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Résumé du poste

IQVIA LLC in Belgium is seeking a Freelance Senior Site Activation Specialist (home-based) to support country-level clinical trial start-up and site management. You will focus on EU-CTR compilation, regulatory submissions, ICF adaptations, and activation, coordinating with cross-functional teams.

The role requires 2–3+ years in site activation or clinical research, a Life Sciences degree, and fluency in Dutch or French and English.

Qualifications

Based in Belgium with strong understanding of the local regulatory environment.
2–3+ years of experience in site activation, study start-up, or clinical research.
Bachelor’s degree in Life Sciences or related field.
Solid knowledge of clinical trial start-up processes and regulatory requirements.
Experience managing site documentation and submission processes.
Strong attention to detail and ability to manage multiple sites and timelines.
Fluent in Dutch or French and English (written and spoken).

Responsabilités

Act as the primary point of contact for assigned investigative sites.
Execute feasibility, site identification, and site activation activities in line with SOPs, regulations, and project timelines.
Prepare, review, and manage essential site and regulatory documents, ensuring completeness and accuracy.
Maintain and update tracking tools, timelines, and internal systems with accurate project data.
Monitor and report on site activation progress and performance metrics.
Ensure compliance with ICH-GCP, local regulations and study requirements.
Collaborate closely with Site Activation Managers, Project Management, and cross-functional teams.