Associate Clinical Research Coordinator Oncology Solid Tumor Research
On-site · Gilbert, Arizona, United States
Job Summary
Coordinate oncology clinical research trials, including consenting participants, data collection and entry, and managing study data across multiple databases. Under supervision, handle operational functions such as patient scheduling, eligibility screening, and maintenance of study records; ensure compliance with Good Clinical Practice, IRB and regulatory requirements; utilize Cerner and electronic data capture systems to populate data, generate reports, and support data quality reviews. May assist in training new staff and support monitoring/audit activities; role operates Mon-Fri 8:00–4:30 with no weekends or holidays, within Banner MD Anderson Cancer Center and Banner Gateway Medical Center networks.
Required Qualifications
- Associate's degree in healthcare, research, or related field
- two years of health care experience or equivalent knowledge/experience in a healthcare or research setting
- knowledge of regulatory affairs and current issues concerning the conduct of clinical research or health care operations
- knowledge of medical terminology and ability to interpret laboratory reports and understand disease processes and testing with an understanding of disease staging and status
- effective interpersonal skills with the ability to provide customer service
- proficient with common office software and ability to conduct computer-based literature searches
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