Conducting and reporting all types of onsite monitoring visits
Driving the study startup phase (if applicable)
Performing CRF reviews, source document verification and query resolution
Responsible for site communication and management
Supervising study activities, timelines, and schedules for each site
Acting as a point of contact for in-house support services and vendors
Supporting quality control, such as compliance monitoring and reports review
Participating in feasibility research
Supporting the regulatory team in preparing documents for study submissions and regulatory approval

BSc or MSc in Life Sciences (or similar)
Independent on-site monitoring experience in Slovakia
Demonstrable experience in all types of monitoring visits in Phase II and/or III
Full and clean driver's license
Fluency in Slovak and English
Experience supporting Oncology studies is beneficial but not essential
Intermediate to Advanced knowledge of MS Office

Freelance Senior Clinical Research Associate

Key skills