MFA / MTA / Pflegefachperson / Dokumentationsassistent für das zentrale Studiensekretariat (m/w/d)
Core
Support clinical trial participants and coordinate documentation for lung cancer clinical trials at a central study center.
Role type
Clinical trial documentation assistant
Builds
Clinical trial documentation and patient scheduling
Domain
Healthcare / Clinical Research
Required skills
Medical assistant training, GCP knowledge, English basics, data entry, document management, medication handling, appointment scheduling, audit preparation
Preferred skills
GCP certification, MS Office proficiency
Responsibilities
Patient and participant support, training participants and colleagues on protocol requirements, managing information flow between sponsors and doctors, transferring data from medical records to documentation forms, organizing and storing trial medication and diagnostics, scheduling patient appointments, coordinating with monitors and study doctors, preparing for visits and audits