Precious Duru
Clinical Research Professional
- Role
- Clinical Studies Coordinator - Regulatory at UT MD Anderson
- Location
- Houston, TX, US
- LinkedIn followers
- 500 followers
About Precious Duru
Clinical research professional with experience supporting Phase clinical trials…
Experience
Clinical Studies Coordinator - Regulatory
Mar 2025 — Present
Assembly of regulatory documents required per local and FDA regulation, departmental andinstitutional standard operating procedures (SOPs) and processes for clinical trial operations(activation, amendments, etc.)-Timely submission of required clinical trial regulatory documents (IND relateddocuments for Compliance Office and oversight of the FDA approval process, etc.)- Performs routine Quality Assurance of regulatory files for assigned clinical trials prior tomonitoring, audit, or inspection visits-Tracks changes and updates in regulatory laws/guidelines as they occur. Discusses andcommunicate changes to appropriate team members, including management. Assists in thecoordination and implementation of changes to department process as necessary
Education
Xavier University of Louisiana
Bachelor of Science - BS
Mississippi College
Master of Science - MS
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