Senior Site Specialist
Core
Senior operational point of contact for investigator sites across the Benelux region, managing site start-up, maintenance, and close-out activities while supporting local regulatory submissions.
Role type
Senior Site Specialist (Clinical Research Operations)
Builds
Clinical trial site operations and regulatory compliance for studies in the Benelux region
Domain
Healthcare / Clinical Research / CRO
Deliverable
client delivery
Required skills
Site support, clinical trial administration, study start-up, regulatory document management, clinical trial management systems, process improvement, mentorship
Preferred skills
CTIS submissions, country-specific regulatory requirements
Technologies
Clinical trial management systems, trackers
Responsibilities
Managing advanced site-level activities including document collection, review, and maintenance; Supporting local study start-up including CTIS submissions and regulatory coordination; Acting as primary liaison for site staff on operational and regulatory questions; Ensuring accurate updates of site status and study data in systems; Coordinating site visits and communications with stakeholders; Identifying opportunities to improve site workflows; Providing guidance and mentorship to junior team members
Seniority
Senior, hands-on IC with mentorship responsibilities
