You will be working at an award-winning biopharmaceutical company focused on developing novel treatments for CNS diseases.
Job Detail
Job Description
Duties:
- Support the internal and external study teams to ensure TMF quality as per regulatory guidelines
- Support document control processes in Veeva eTMF including filing, review of documents for accuracy, completeness and legibility, review of deletion requests as well as resolution of quality issues
- Perform audit of TMF documentation, provided findings to the clinical team and supported the team in resolution of issues
- Support the clinical study teams with study eTMF Milestones and EDLs
- Perform final eTMF processing and reconciliation in preparation for study close-out and archival
Requirements:
- Bachelor's Degree
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- Great opportunity in beautiful Florida and great benefits!