Clinical Study Administrator(CTA)
Parexel(1 month ago)
About this role
A Clinical Trial Administrator at Parexel supports the coordination and administration of clinical studies from start-up through closeout, focusing on regulatory and essential study document management. The role maintains the local eTMF and ISF, facilitates submissions to ethics committees and regulatory authorities, and acts as a primary local administrative contact for investigators, CRAs, and vendors.
Required Skills
- Document Management
- Regulatory Submissions
- eTMF
- ISF Maintenance
- CTMS
- Stakeholder Liaison
- Meeting Coordination
- Archiving
- Quality Compliance
- Translation Support
About Parexel
parexel.comFor over 35 years Parexel has been a trusted global CRO and biopharmaceutical services company. Learn more about how we can help.
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