- Seattle, Washington, United States
- On-site
- Full-time · Associate
- $33–$49 per hour
- 2–3 years
The Clinical Research Coordinator II is responsible for day-to-day coordination of interventional Phase I-III clinical trials and observational Cancer Control studies, overseeing subject-level study workflows from screening to data reporting.
Compensation
The hourly pay range for this position is from $32.63 to $48.93 and pay offered will be based on experience and qualifications.
Responsibilities
- Conduct daily clinical operations of assigned research studies in accordance with study protocols, regulatory and GCP guidelines, and institutional policy.
- Develop and maintain tools for study implementation, including data collection tools, reference materials, and specific study orders.
- Provide study-specific education and training to clinic staff, participants, and other stakeholders.
- Coordinate patient enrollment and participation by reviewing study candidates' medical records for eligibility, initiating enrollment, ensuring informed consent, and maintaining accurate enrollment records.
- Schedule patient clinic visits and ongoing study visits; ensure administrative compliance with study protocols.
Requirements
- High school diploma or equivalent
- Associate's or bachelor's degree in a healthcare, life sciences, public health, or related field
- Nice to have: Certified Clinical Research Coordinator (CCRC)
- Nice to have: Certified Clinical Research Professional (CCRP/SOCRA)
- Nice to have: Experience working with NIH, FDA, OHRP, and ICH-GCP regulations