Clinical Study Administrator
Core
Administrative support for clinical research teams to ensure accurate Trial Master File delivery and site compliance tracking.
Role type
Administrative Support Specialist (Clinical Research)
Builds
Trial Master Files (TMF) and clinical documentation systems
Domain
Clinical Research / Life Sciences
Deliverable
dashboards & analysis
Required skills
Clinical Trial Supplies management, Case Report Forms (CRFs) tracking, Clinical data flow management, Trial Master File (TMF) maintenance, Clinical documentation filing and archiving, Project communication coordination, Site visit support
Preferred skills
Good Clinical Practice (GCP) knowledge, International Conference on Harmonization (ICH) guidelines knowledge, Protocol requirements knowledge
Technologies
Microsoft Word, Microsoft Excel, Microsoft PowerPoint
