Clinical Trials Assistant, Sponsor Dedicated
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 (Sponsor Dedicated)
Builds
Trial Master Files (TMF), clinical documentation, and clinical trial supply tracking.
Domain
Clinical Research / Life Sciences
Required skills
Clinical Trial Management, Trial Master File (TMF) maintenance, Clinical Trial Supplies management, Case Report Form (CRF) coordination, Regulatory guidelines knowledge (GCP/ICH), Microsoft Office proficiency
Preferred skills
Site visit accompaniment experience, Protocol requirements knowledge
Responsibilities
Update and maintain clinical documents and systems, prepare and archive clinical documentation, review study files for completeness, coordinate clinical trial supplies and data flow, act as central contact for project communications
Seniority
Entry-level to Junior (1+ years experience required)
