12 years of experience as a Clinical Research Coordinator with a primary focus on data entry and query resolution for oncology trials.
12 years of oncology clinical research experience
Experience screening, enrolling, and consenting patients into research studies based on study protocols.
Experience with adverse event reporting, including identification, documentation, and communication of AEs and SAEs.
Proficiency using Oncore for clinical trial management and reporting.
Proficiency with Microsoft Excel and Word for creating and maintaining study tools and documentation.