Kelly Murney

About Kelly Murney

Research professional with a Bachelor of Arts (B.A.) focused in Sciences, Healthcare, and…

Experience

1. Clinical Research Associate Ii

   Rho

   May 2024 — Present

   Provides on-site monitoring of clinical trials of varying size.• Reviews regulatory documents, as required, and prepares site visit reports.• Identifies and resolves problems at assigned investigative sites to ensure subject safety and the highest possible data quality.• Monitors drug accountability.• Tracks site action items to resolution.• Conducts business in accordance with Rho SOPs, FDA regulations, and ICH/GCP guidelines.• Conducts interim-monitoring visits, to ensure the integrity and quality of clinical data with respect to accuracy, documentation, and methods through the review of CRFs, source documents, medical records, drug accountability logs and regulatory documents.• Conducts site close-out visits for the purpose of inventory and return of clinical supplies, monitors remaining CRFs, resolves outstanding issues, and details document retention policy with the investigator.• Provides verbal and written feedback to study sites regarding overall performance and deficiencies.• Prepares monitoring visit reports and communicates findings to the Sponsor, site personnel, the Rho Clinical Operations management, and the Rho Project Manager.• Reviews regulatory documents internally as well as on site to ensure compliance with FDA regulations and guidelines.• Executes timely and accurate completion of all monitoring visit reports, and ensures effective follow up and resolution of site issues.• Resolves CRF queries from sites in a timely manner in order to meet projects.

Education

• Arizona State University

  Bachelor of Arts (B.A.)

• Clinical Research Fastrack

  Certificate of Completion

Skills

• Microsoft Word
• Public Speaking
• Caregiving
• Microsoft Powerpoint
• Microsoft Office
• Bls Instruction
• Customer Service
• Research
• Teaching
• Time Management
• Healthcare
• Microsoft Excel
• Bls