Clinical Research Coordinator 2
$75,000–$90,000 year
On-siteSeattle, Washington, United States
Job Summary
Recruit, prescreen, and obtain informed consent from prospective study participants while conducting clinical study visits that include medical history collection, protocol-specified procedures, phlebotomy, and source data recording. Collect, process, and prepare specimens according to clinical and laboratory protocols, then maintain screening logs, enrollment logs, and participant records. Enter and validate study data into electronic data capture platforms, support data cleaning and query resolution, and maintain regulatory documents for the Study Master File. Travel to partner laboratories, at-home collection sites, and clinic locations to support enrollment and data collection, with occasional travel estimated up to 10%.
Required Qualifications
- Authorized to work in the United States
- Primarily on-site in Seattle five days per week
- Bachelor's Degree in a biological or health science field
- At least two years of experience in a clinical research coordinator or comparable role
- Medical Assistant Phlebotomist certification for Washington State, or readiness to obtain it
- Working knowledge of medical terminology, clinical trials, and Good Clinical Practice (GCP)
- Comfort working with clinical/laboratory data and research data systems
- Ability to work both independently and as part of a distributed team
- Able to lift and handle laboratory shipments and supplies as needed
- Occasional travel to partner laboratories or study sites may be required (estimated up to 10%)
Desired Qualifications
- Experience with EDC platforms
- Phlebotomy certification preferred (to be completed within 30 days of hire if not already held)
- GCP and IATA training (to be completed within 30 days of hire if not already held)
- Proficiency with Microsoft Office and willingness to learn other research systems, e.g., EDC
- Proficiency with Microsoft Office and willingness to learn research inventory and data systems
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