Clinical Research Data Specialist / Clinical Research Data Specialist II, UC Cancer Center

Essential Functions: Follow established CTO workflows and CTO/UC Health standard operating procedures. Proactively review and locate source documentation for all study procedures. Accurately enters data from source documentation into electronic data capture (EDC) systems within 5 days of the patient visit. Proactively seeks to promptly resolve outstanding data queries and any issues through collaboration with clinical research coordinators (CRCs).Maintains and uses organizational systems to avoid delinquent data entry. Reviews all data entered into EDCs and subject charts to identify and help resolve any general quality issues. Conducts study participant follow-up as required per protocol. Communicates and collaborates within assigned research team and with principal investigators in a professional, helpful, and service-oriented manner. Acts as the primary point of contact for monitoring visits. Adheres to all UCCC CTO work instructions, SOPs, and study specific timeframes. Able to independently maintain and meet form & database development milestones. Maintain/Update patients' status in the Clinical Trial Management System. Maintain Team's biospecimen collection kit inventory, re-ordering supplies as needed.

Compensation and Benefits: UC offers an exceptional benefits package designed to support your well-being, financial security, and work-life balance. Highlights include: Comprehensive Tuition Remission Robust Retirement Plans Real Work-Life Balance

Additional Benefits Include: Competitive salary based on experience Comprehensive health coverage (medical, dental, vision, prescription) Flexible spending accounts & wellness programs Professional development & mentorship opportunities To learn more about why UC is a great place to work, please visit our Careers Page.