Bachelor's degree in Science, Healthcare, or a related field.
Minimum of 4 years of clinical research experience OR 2+ years in a Senior Clinical Data Coordinator or Senior Regulatory Specialist role.
Strong understanding of clinical research regulations and study conduct.
Experience supporting Principal Investigators and clinical study teams.
Excellent organizational, communication, and documentation skills.
Ability to manage multiple studies and deadlines in a fast-paced environment.
Proficiency in Microsoft Office and/or Google Workspace.
Experience with oncology, specialty, or investigator-initiated research studies.
Experience with IRB submissions, sponsor interactions, and site monitoring visits.
Strong patient-facing clinical research experience.