Clinical Research Coordinator I

Fred Hutchinson Cancer Center•Seattle, WA

4d•Onsite

About The Position

The Clinical Research Coordinator I helps to organize and carry out day-to-day operations and administrative functions of investigator-initiated and industry-sponsored human subjects clinical trials. This individual will work under general supervision of the Principal Investigator, Clinical Research Nurse or Clinical Research Manager and will be required to perform his/her responsibilities with limited degree of independence within the scope of study protocol(s) and institutional policies and guidelines.

Requirements

High school diploma or equivalent.
Minimum one year experience in a clinical research or cancer registry environment with regulatory or human research protections.
Demonstrated knowledge of how to synthesis study conduct.
Ability to apply judgement in interpreting regulations, determining impacts, and knowing when to escalate questions and concerns when appropriate.

Nice To Haves

Associate or bachelor’s degree preferred.
Certified Clinical Research Coordinator (CCRC) or certification as Clinical Research Professional (SOCRA).
Experience with REDCap or other databases.
Ability to work with multiple data management systems including generating reports and sourcing data from systems.

Responsibilities

Provide day-to-day coordination of sample acquisition studies including identifying eligible patients.
Consent patients onto sample acquisition studies, confirming informed consent has been properly obtained, collect data, and communicate with other study staff.
Work in collaboration with principal investigator and study staff to ensure that patients are enrolled on studies in an efficient manner.
Partner with clinic staff to ensure procedures are scheduled appropriately.
Place orders for the collection of study samples.
Track patients' locations and coordinate sample collection appointments with patients in both the inpatient and outpatient settings.
Develop and implement data tracking systems, ensuring hard copy and computer files are regularly and accurately maintained.
Enter sample data into sample tracking database.
Ensure samples are transported to the appropriate receiving lab.
Other duties as assigned.