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Clinical eTMF Specialist
Job description
The Clinical eTMF Specialist is responsible for the management, oversight, and quality control of the electronic Trial Master File (eTMF) throughout the lifecycle of clinical trials. This role ensures compliance with Good Clinical Practice (GCP), ICH guidelines, company Standard Operating Procedures (SOPs), and regulatory requirements.
The specialist will collaborate with internal teams, CROs, and study sites to maintain inspection readiness and ensure accurate, complete, and timely documentation within the eTMF system.
Description copied from Artivion's careers page. Read the full posting before you apply.
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