Fred Hutchinson Cancer Research Center Clinical Research Coordinator II in Kirkland, Washington
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 functions independently at SCCA's clinic on the EvergreenHealth campus in Kirkland. This coordinator participates in all aspects of clinical research trials except those that require medical expertise or licensure and leads key tasks such recruitment/screening/enrollment, supporting the managment of patients being treated in a clinincal trial, 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 protocol implementation
Minimum of 2 years of experience in a clinical research setting required
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
Oncology research experience preferred
Bachelor's degree or 2 years of clinical 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.
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