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Role Overview:
- Senior-level contract role managing clinical trial documentation.
- Fully remote US position ensuring inspection-ready TMF quality.
Key Accountabilities:
- Upload, review, and reconcile documents in the Trial Master File.
- Manage user access, completeness checks, and CRO oversight activities.
Requirements:
- Bachelor's degree and 5+ years of TMF experience.
- Knowledge of GCP, ICH, and CDISC TMF Reference Model.