The purpose of this position is to implement and support research activities at Seattle Cancer Care Alliance Network sites. The Clinical Research Coordinator (CRC) III will be responsible for coordinating all aspects of oncology clinical research trials and will act as a lead CRC for the department. The person in this role will also participate in team development activities such as training, quality assurance, and procedures and tools creation.
- 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 - Develops or creates 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 - Develops department and/or protocol standard operating procedures, work instructions, and tools - Leads the startup of a study including things such as budget development, contracting, and protocol implementation - Serves as an education and training resource to others in the ongoing development of clinical research knowledge and experience - Provides overall quality assurance of clinical research for the department - Take meeting minutes and distribute as appropriate - Lead monthly teleconferences/meetings - Attend disease specific research meetings/events
Minimum of 5 years of experience in a clinical research setting required Oncology research experience preferred Certified Clinical Research Coordinator (ACRP), Certified Clinical Research Professional (SOCRA), or equivalent certification
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