University of Washington Seattle, WA Full-time Research
Posted on March 26, 2020
|Job Location:||Seattle Campus|
|Closing Info:||Open Until Filled|
|Salary:||Salary is commensurate with experience and education|
UW faculty and staff also enjoy outstanding benefits, professional growth opportunities and unique resources in an environment noted for diversity, intellectual excitement, artistic pursuits and natural beauty. All of which has allowed the UW to be nationally recognized as a “Great College to Work For” for six consecutive years.
The Division of Cardiology is a large, complex Division in the Department of Medicine with over 100 faculty, 31 fellows and over 100 professional, classified and hourly employees spread across 6 campuses: UW, Harborview Medical Center, Northwest Hospital, Edmonds Cardiology Clinic, VA Puget Sound Hospital and UW South Lake Union. The Division of Cardiology physicians address the prevention and treatment of heart and vascular disease through the investigation of new technologies, drugs, and devices that ultimately translate into best practices and improvement of patient care.
The Division of Cardiology has an outstanding opportunity for a full-time Regulatory Research Coordinator. The Clinical Trials Unit (CTU) at the University of Washington supports investigators by providing a sound clinical research infrastructure and ensuring research participant safety, compliance with federal, state and institutional regulations, policies, and procedures. The CTU provides investigator support on all aspects of heart and vascular disease for investigator initiated, government, and industry sponsored clinical research studies. The CTU supports and manages Human Subjects, regulatory, and financial oversight to ensure efficient execution of studies with the highest quality data.
Position Dimensions and Impact to the University:
This position requires an in-depth knowledge of protocol requirements, good clinical practices as set forth by federal regulations, and financial management. As the primary expert for clinical research regulations, the Regulatory Research Coordinator will facilitate the implementation and post award maintenance of clinical trials. This individual will assist with IRB submissions, the maintenance of regulatory files, development of study budgets in conjunction with the CRBB, tracking study reimbursements, and other contract and budget requirements as set forth my OSP and UW Compliance.
Duties & Responsibilities:
The major duties can be categorized in 3 major areas: study project management, communications management, and other duties as required.
Study Project Management
Undergo required Human Subjects Training and Good Clinical Practice (GCP) training.
As a UW employee, you will enjoy generous benefits and work/life programs. For detailed information on Benefits for this position, click here.
Equivalent education/experience will substitute for all minimum qualifications except when there are legal requirements, such as a license/certification/registration.
CONDITIONS OF EMPLOYMENT
The application process for UW positions may include completion of a variety of online assessments to obtain additional information that will be used in the evaluation process. These assessments may include Workforce Authorization, Cover Letter and/or others. Any assessments that you need to complete will appear on your screen as soon as you select “Apply to this position”. Once you begin an assessment, it must be completed at that time; if you do not complete the assessment you will be prompted to do so the next time you access your “My Jobs” page. If you select to take it later, it will appear on your "My Jobs" page to take when you are ready. Please note that your application will not be reviewed, and you will not be considered for this position until all required assessments have been completed.