Clinical Study Coordinator
5 days ago
Summary of Responsibilities:
- Assist in setting up and maintaining tracking systems/spreadsheets for study supplies.
- Maintain Trial Master File documentation within the appropriate TMF platform, participate in TMF QC, as assigned, and track and archive as applicable.
- Audit and CAPA tracking.
- Liaise with vendors, as needed, for study conduct such as printing study materials and/or external systems access for study team members.
Required Skills and Qualifications:
- Diploma – Associate degree or equivalent.
- Good oral and written communication skills.
- Computer literacy (Microsoft Office Suite: Word, Excel, PowerPoint).
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