Clinical Research Coordinator II


  • Location: Seattle, WA
  • Posted: Dec 6, 2019

Job Description


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.
Responsibilities
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

Qualifications


Required:
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
Preferred:
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.
Our Commitment to Diversity
We are proud to be an Equal Employment Opportunity (EEO) and Vietnam Era Veterans Readjustment Assistance Act (VEVRAA) Employer. We are committed to cultivating a workplace in which diverse perspectives and experiences are welcomed and respected. We do not discriminate on the basis of race, color, religion, creed, ancestry, national origin, sex, age, disability (physical or mental), marital or veteran status, genetic information, sexual orientation, gender identity, political ideology, or membership in any other legally protected class. We are an Affirmative Action employer. We encourage individuals with diverse backgrounds to apply and desire priority referrals of protected veterans. If due to a disability you need assistance/and or a reasonable accommodation during the application or recruiting process, please send a request to our Employee Services Center at escmail@fredhutch.org or by calling 206-667-4700.

Employment Type


  • Regular Full-Time