About Me
Clinical research professional with 8+ years of experience supporting and managing clinical trials across academic, hospital, and international research settings. Skilled in study start up through closeout, regulatory submissions, IRB and ICH GCP compliance, patient recruitment and informed consent, audit readiness, and data integrity across EDC and CTMS platforms. Experienced in medical device and therapeutic trials across multiple specialties, with a strong track record of ensuring compliance, streamlining workflows, and supporting high quality research outcomes. Holds a Master’s degree in Clinical Research Administration from Eastern Michigan University and is passionate about advancing ethical, patient centered research while collaborating with sponsors, CROs, and healthcare teams to deliver reliable and impactful clinical results.
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