Certified Clinical Research Coordinator (CCRC) with 7+ years of experience managing Phase 1–4 clinical trials, including drug/device studies and urologic oncology research. Skilled in study conduct, regulatory compliance, data management, and study protocol adherence, with a proven track record of exceeding enrollment goals and passing multiple FDA audits. Passionate about clinical research and dedicated to ensuring participant safety and adherence to Good Clinical Practice (GCP) standards. Strong communication and leadership skills, with a personable approach that excels in building relationships with multidisciplinary teams and leading collaborative efforts to drive successful trial outcomes. Excited to apply my skills and experience in clinical research to advance my career and transition into a Clinical Research Associate (CRA) role.
Responsibilities Include:
Responsibilities Included:
Responsibilities included: