Now operating with additional safety precautions for COVID-19


Seattle Women's: Health, Research, Gynecology is seeking a full-time
Clinical Research Coordinator to join our team.

Our Mission: Seattle Women’s: Health, Research, Gynecology® is dedicated to providing exemplary health care for women of all ages. We offer a unique practice that integrates preventative care and medical treatment in addition to cutting-edge research. Our approach creates a standard of excellence in the specialized care of women.
The Clinical Research Coordinator (CRC) serves as an integral member of the research team and will work closely with members of Seattle Women’s staff across the organization. The Clinical Research Coordinator reports primarily to the Executive Director. The ideal candidate will combine clinical research experience with excellent communication skills and the ability to manage multiple projects with strong attention to detail.
The CRC’s main responsibility is the conduct of multiple clinical trials. CRC’s will work closely with research subjects, the Principal Investigator, Sub-Investigators, and Sponsors/CROs to ensure that each study is conducted properly per protocol and Good Clinical Practice. 


Essential Job Functions will include, but are not limited to:                                          

  • Screening and recruitment of potential study participants
  • Conducting informed consent discussions
  • Collecting vitals and medical history
  • Tracking clinical trial subjects and scheduling follow-up assessments
  • Developing and organizing regulatory documents
  • Communicating with the IRB
  • Performing all coordinator-mediated tasks, per individual protocols
  • Drug accountability and reconciliation
  • Processing and packaging specimens, per IATA guidelines

In order to be successful at this position, you should:

  • Have at least one year of experience as a Clinical Research Coordinator (CRC)
  • Have experience with direct patient care, preferably in the field of women’s health
  • Have experience in conducting an informed consent discussion
  • Have experience obtaining medical history and basic vital signs
  • Show proficiency in MS Office and basic computer skills
  • Have experience with the use of electronic case report form (eCRF)
  • Be organized, flexible, and willing to step in where needed
  • Have attention to detail
  • Be self-motivated and a fast learner

Preferred requirements

  • Have a Bachelor’s degree
  • Phlebotomy experience
  • Processing and packaging lab specimens in compliance with IATA guidelines
  • Training in HIPAA, Good Clinical Practices (GCP) and Human Research Protection
Please apply via LinkedIn if you are interested.