Clinical Research Assistant - Lacey
About The Position
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.
Requirements
- Washington Medical Assistant Phlebotomist Certification
- One (1) year Experience as a Medical Assistant or Laboratory Assistant performing phlebotomy and CLIA waived testing in a clinical setting.
- Clinical research experience in oncology.
Nice To Haves
- Medical Assistant or Phlebotomy training program/course approved by Washington State.
- Graduate of an accredited school for medical assistants, or an equivalent combination of coursework and experience/training sufficient to qualify to sit for the Washington State Certification exam.
Responsibilities
- Facilitate all aspects of clinical research within the Providence Swedish Cancer Institute in South Puget Sound.
- Work 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.
- Coordinate study timelines and resources.
- Ensure accurate collection and submission of research data to sponsors.
- Support regulatory compliance through informed consent preparation, regulatory documentation, adverse event and protocol deviation reporting, and continuing review activities.
- Ensure efficient study operations, data integrity, and timely completion of clinical trials.
Benefits
- Best-in-class benefits are uniquely designed to support you and your family in staying well, growing professionally, and achieving financial security.
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
No Education Listed
Number of Employees
501-1,000 employees
