Clinical Research Coordinator I, Cancer and Hematology Clinical Research Program

Responsibilities: Evaluate patient eligibility for research studies and screen for enrollment Conduct telephone interviews and schedule study visits Obtain informed consent for non-treatment studies and register patients to cohorts/protocols Review and abstract medical records, including pathology reports Access and input data into EMR and eCRF systems and other departmental systems Ensure data quality and completeness, respond to queries Perform clinical tests (phlebotomy, EKGs) Coordinate collection, processing, and storage of biological specimens May manage IRB/submissions and regulatory file maintenance Maintain ongoing communication with research managers and PIs for data needs Carry out administrative tasks, mailings, inventory, and equipment setup Support audits and other compliance activities

Key requirements: Bachelor Experience in clinical research (preferred) Experience with subject recruitment and understanding of ethical/technical conduct of research (preferred) Excellent English communication (oral and written) Cultural sensitivity and comfort with diverse populations Proficiency with Microsoft Office and web browsers Ability to maintain strict confidentiality of health information strong communication cultural sensitivity attention to detail MS Word MS Excel MS Access