Overview

Freelance clinical research professional, Sr. CRA / Lead CRA with broad experience; hands-on, can-do attitude; having oversight whilst keeping attention to details. | study start up | regulatory and EC Submissions | lead CRA | routine monitoring | writing of project specific plans (Monitoring, DSMB, CEC) | audit preparation and follow-up | safety reporting | (e)CRF development | training of site staff and CRAs | medical device, pharma and nutrition | phase I - IV |