EPIC
Experienced clinical research professional with a strong history of supporting clinical trials in compliance with regulatory protocols and GCP standards. Skilled in data extraction, source verification, and identifying patient safety or data inconsistencies. Adept at coordinating patient records, lab specimens, and regulatory documentation across multiple studies. Known for being highly organized, analytical, and solution-oriented, with proven strengths in team collaboration, adaptability, and strategic planning.
Office administration
Strong organization
Electronic data capture
Clinical research ethics
Clinical trial management
Regulatory submissions
Source document verification
Documentation management
Laboratory results management
Adverse event tracking
Patient education
Adaptability and flexibility
Time management abilities
EPIC
NextGen
CERNER
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