Clinical Research Coordinator

The Clinical Trials Coordinator facilitates all aspects of clinical research within the Providence Swedish Cancer Institute in South Puget Sound. This role works collaboratively with sponsors, investigators, regulatory and contract teams, and the Institutional Review Board (IRB) to support the initiation, conduct, and close-out of clinical trials. Responsibilities include coordinating study timelines and resources, ensuring accurate collection and submission of research data to sponsors, and supporting regulatory compliance through informed consent preparation, regulatory documentation, adverse event and protocol deviation reporting, and continuing review activities.

The coordinator plays a key role in ensuring efficient study operations, data integrity, and timely completion of clinical trials.

• Associate's Degree in Healthcare related field.

• Bachelor's Degree in Healthcare related field.
• upon hire: ACRP, or SOCRA certification (or equivalent), current CITI HSP, GCP, and COI.
• Two years of clinical research experience.

Our best-in-class benefits are uniquely designed to support you and your family in staying well, growing professionally, and achieving financial security. We take care of you, so you can focus on delivering our Mission of caring for everyone, especially the most vulnerable in our communities.

Accepting a new position at another facility that is part of the Providence family of organizations may change your current benefits. Changes in benefits, including paid time-off, happen for various reasons. These reasons can include changes of Legal Employer, FTE, Union, location, time-off plan policies, availability of health and welfare benefit plan offerings, and other various reasons.