Seattle Cancer Care Alliance
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Clinical Research Coordinator II
at Seattle Cancer Care Alliance
- Job ID
- Regular Full-Time
- Seattle Cancer Care Alliance
The Seattle Cancer Care Alliance (SCCA), located in Seattle, Washington, is part of a dynamic collaboration among three organizations known nationally and internationally for their patient care and research: Fred Hutchinson Cancer Research Center, University of Washington, and Seattle Children's. Over the past 25 years, these institutions have worked together to support their mission of adult and pediatric oncology patient care services, research and education.
The Clinical Research Coordinator II participates in all aspects of clinical research trials except those that require medical expertise or licensure and leads key tasks such accurate record keeping, data collection and management, and correspondence.
- Provides day-to-day coordination of clinical research studies including screening patients for protocol eligibility, ensuring informed consent has been properly obtained, enrolling subjects,collecting data and communicating with clinic staff
- Collaborates with clinic providers and staff, ancillary services, and research staff regarding protocol implementation and operations
- Collects and enters data in a timely manner in accordance with the protocol
- Collects and maintains regulatory documents
- Submits reports and documents as required
- Coordinates the study drug management process
- Coordinates research protocol monitoring and auditing visits and takes action to correct problems such as deviation from protocol requirements to ensure research quality
- Participates in the development of department and/or protocol standard operating procedures and tools
- Participates in the startup of a study including things such as budget development, contracting, and protocol implementation
- Minimum of 2 years of experience in a clinical research setting
- Proficiency with email, spreadsheets, word processing, and databases
- Experience with electronic medical records systems
- Ability to understand and follow multiple complex protocols at multiple sites
- Ability to organize and manage time and tasks independently
- Ability to develop and/or present content to senior leaders and other groups
- Problem solving skills
- Bachelor's degree or 2 years of clinical research experience
- Oncology research experience
- Certified Clinical Research Coordinator (ACRP), Certified Clinical Research Professional (SOCRA), or equivalent certification
- Knowledge of regulations and guidelines for conducting clinical research; for example, good clinical practice (ICH-GCP), Human Subjects Protocol, etc.