Clinical Trials Assistant (1 Year Contract)
Core
Administrative support for Clinical Research Associates and Regulatory teams to ensure accurate Trial Master File delivery and site compliance tracking.
Role type
Clinical Trials Assistant (CTA)
Builds
Trial Master Files (TMF), clinical documentation, and study file records
Domain
Clinical Research / Life Sciences
Required skills
Clinical Trial Assistant experience, English proficiency, Microsoft Office (Word, Excel, PowerPoint), GCP/ICH guidelines knowledge, protocol requirements knowledge, document management, data tracking
Preferred skills
1+ year CTA experience in CRO/pharma, site visit accompaniment capability
