Remote Site Activation Coordinator (Belgium)

IQVIA Argentina; Zaventem; Hybride; EUR 45 000 - 65 000; Plein temps

Résumé du poste

IQVIA Belgium is seeking a Site Activation Coordinator to support country-level activation activities for clinical trials, with homebased work and occasional travel to Zaventem. You will work under SOPs, review regulatory documents and coordinate with SAM, PM, and other teams to ensure timely site activation.

Fluent English, Dutch and French are required; healthcare trials experience preferred. The role offers exposure across multiple therapeutic areas in a global network and opportunities for

Qualifications

• 2 years’ minimum experience in a healthcare environment supporting clinical trials.
• Exposure to site activation activities preferred.
• Must speak strong English, Dutch and French.

Responsabilités

• Under general supervision, perform feasibility, site activation and some maintenance activities in assigned studies for investigative sites, according to applicable regulations, SOPs and work instructions, working closely with the Site Activation Manager (SAM), Project Management team, and other departments as necessary.
• Prepare site documents, reviewing for completeness and accuracy.
• Inform team members of completion of regulatory contractual and other documents for individual sites.
• Distribute completed documents to sites and internal project team members.
• Support the updating and maintenance of internal systems, databases, tracking tools, timelines and project plans with accurate and complete project specific information.
• Review, track and follow up the progress, the approval and execution of required documents such as questionnaires, CDAs, regulatory, ethics, Informed Consent Forms and Investigator Packs release documents.

Connaissances

English

Dutch

French

Description du poste

IQVIA Belgium is seeking a Site Activation Coordinator to support country-level activation activities for clinical trials, with homebased work and occasional travel to Zaventem. You will work under SOPs, review regulatory documents and coordinate with SAM, PM, and other teams to ensure timely site activation.

Fluent English, Dutch and French are required; healthcare trials experience preferred. The role offers exposure across multiple therapeutic areas in a global network and opportunities for