Raven Boyd

I coordinate and execute clinical trials at the site level in compliance with study protocols, ICH-GCP guidelines, and FDA regulations. I screen and enroll participants, obtain informed consent, conduct study visits (vital signs, ECGs, phlebotomy, and physical assessments), and monitor/report Adverse Events and Serious Adverse Events to the PI, Sponsor, and IRB.

I also bring a strong laboratory background—from specimen processing and accessioning to cytology/histology support—using systems like Athena LIS and supporting accurate test code entry. I maintain regulatory and study documentation (including IRB submissions, protocol amendments, and continuing reviews) and ensure data integrity through timely source documentation and EDC query resolution.

I’m recognized for organization, attention to detail, communication, and problem-solving, including preparation for and support of monitoring visits, audits, and inspections. I’m currently pursuing a B.S. in Health Science through Western Governors University.