CTA2
Core
Administrative support for Clinical Research Associates and Regulatory teams to ensure accurate Trial Master File delivery and clinical documentation management.
Role type
Administrative Clinical Research Coordinator
Builds
Trial Master Files (TMF), clinical documentation, and clinical trial supply tracking
Domain
Clinical Research / Life Sciences
Required skills
Clinical Trial Supplies management, Case Report Forms (CRFs) tracking, Clinical data flow coordination, Trial Master File (TMF) maintenance, Clinical documentation filing and archiving, Regulatory guideline knowledge (GCP/ICH), Microsoft Office proficiency
Preferred skills
Clinical research experience, Site visit accompaniment
Technologies
Microsoft Word, Excel, PowerPoint
Responsibilities
Update and maintain clinical documents and systems, Prepare and archive clinical documentation, Review study files for completeness, Coordinate clinical trial supplies and CRFs, Act as central contact for project communications
Seniority
Mid-level, administrative support
