Clinical Research Coordinator I - ASCEND Program
$53,498–$76,170 year
On-siteSeattle, Washington, United States
Job Summary
Review study candidates' medical records for eligibility, initiate scheduling of clinic and ongoing study visits, and attend participant visits to ensure clinical procedures and protocol-specific activities are completed. Serve as a liaison for Investigational Drug Services regarding drug assignment and dispensation, perform non-clinical ECGs, administer study questionnaires, and maintain accountability for study drug self-administration. Coordinate research protocols within Fred Hutch and UW clinic settings, document study-related activity in Epic EHR, eReg, and CTMS, and respond to data queries from monitors. Identify and report adverse events per regulatory guidelines, transport laboratory samples, and provide back-up for Data Coordinators as needed. This two-year paid training and mentorship program includes onboarding, monthly professional development, and Year 2 support for graduate or medical school applications for eligible participants.
Required Qualifications
- Associate or bachelor's degree in a related field
- Organizational skills
- Attention to detail
- Ability to problem solve
- Ability to prioritize multiple competing tasks in a dynamic environment
- Excellent written and oral communication skills
- Leadership ability
- Flexibility to work in collaboration with a multi-disciplinary team
- Onsite work is required for patient visits
Desired Qualifications
- Minimum of 1 year of research or related experience
- Previous experience in oncology research
Hiring someone like this?
Get your role in front of qualified candidates on Sorce.