Clinical Research Coordinator I/II
$56,181–$79,976 year
On-siteSeattle, Washington, United States
Job Summary
Manage daily clinical operations of assigned oncology studies by reviewing candidate medical records for eligibility, ensuring informed consent, and initiating patient enrollment. Coordinate patient visits, schedule clinic appointments, and attend visits to complete protocol-specific activities including lab tests and non-clinical assessments. Administer study drugs, perform ECGs, and maintain drug accountability while collaborating with Investigational Drug Services. Track adverse events, respond to study monitor queries, and file all research documentation in patient charts. Work partially on campus and remotely, with flexible hours driven by variable patient visit schedules.
Required Qualifications
- High school diploma or equivalent
- Minimum one year experience in a clinical research or cancer registry environment with regulatory or human research protections
- Demonstrated knowledge of how to synthesize study conduct
- Ability to apply judgement in interpreting regulations, determining impacts, and knowing when to escalate questions and concerns when appropriate
- Minimum two to three years' experience in a clinical research or cancer registry environment with regulatory or human research protections
- Flexibility with work schedule as needed: in-person work will be driven by research patient visits, which will be variable. Managing patient visits may occur before or after regular work hours and some on the weekends
Desired Qualifications
- Bachelor's degree or equivalent experience
- Previous experience in oncology research
- Previous experience with EPIC Electronic Medical Records
- Prior exposure to CTMS, Florence, and/or EDC platforms
- Knowledge of clinical trials records, procedures, and computerized data processing systems
- Excellent organizational skills, attention to detail, ability to problem-solve and to prioritize multiple competing tasks in a dynamic environment
- Minimum five years of experience in a research environment with regulatory or human research protections
- CCRP or CCRC accreditation
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