Clinical Study Documentation Specialist
Caris Life Sciences(12 days ago)
About this role
The Clinical Study Documentation Specialist supports clinical research trials by maintaining study documentation, coordinating submissions, and ensuring regulatory compliance. They facilitate communication among research teams, sites, and oversight entities to support successful study progression.
Required Skills
- clinical Documentation
- IRB Submissions
- GCP
- Regulatory Compliance
- Clinical Research
- Microsoft Office
- Study Coordination
- Document Management
- CTMS
- Regulatory Processes
Qualifications
- Associates degree
About Caris Life Sciences
carislifesciences.comCaris fulfills the promise of precision oncology through advanced laboratory testing, including tumor profiling and blood-based cancer diagnostics.
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