Entry-Level Clinical Research Specimen Processor

Fred Hutch

Seattle (WA)

On-site

USD 85,403,000 - 121,464,000

Full time

14 days+
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Benefits offered by this job

Medical/Vision
Dental
Flexible spending accounts
Life
Disability
Retirement
Employee assistance program
Onsite health clinic
Tuition reimbursement
Paid vacation
Paid sick leave
Paid holidays
Paid parental leave

Job summary

Fred Hutchinson Cancer Center in Seattle is seeking an entry-level Shared Resources Specialist I – Clinical Research Specimen Processing to support investigators. You will handle and process clinical specimens, maintain chain of custody, operate lab instruments, and prepare data summaries as part of a growing team.

The role emphasizes collaboration, accuracy, and regulatory compliance, with an 11am–7:30pm shift and a rotating closing shift. 1:30–10pm once every 5–6 weeks. Hours may vary by need.

Qualifications

  • Bachelor’s degree in any field of education.
  • Associate Degree and 1+ years of experience; Or GED/ High School Diploma and 3+ years of experience.
  • Demonstrated ability to learn and adapt to new protocols and techniques.

Responsibilities

  • Research support under supervision and processing clinical research specimens.
  • Establish and maintain collaborative relationships with faculty and external users.
  • Operate and maintain lab instrumentation and perform data calculations.
  • Prepare charts, graphs and summaries; document laboratory activities and data.
  • Provide regulatory and compliance support for the shared resource.
  • Perform administrative tasks including reporting results and basic billing.

Skills

Communication skills
MS Office
Record keeping
Team collaboration

Education

Bachelor’s degree (any field)
Associate Degree + 1+ years experience
GED/ High School Diploma + 3+ years experience

Tools

Specimen processing equipment
Biosafety protocols

Job description

Fred Hutchinson Cancer Center in Seattle is seeking an entry-level Shared Resources Specialist I – Clinical Research Specimen Processing to support investigators. You will handle and process clinical specimens, maintain chain of custody, operate lab instruments, and prepare data summaries as part of a growing team.

The role emphasizes collaboration, accuracy, and regulatory compliance, with an 11am–7:30pm shift and a rotating closing shift. 1:30–10pm once every 5–6 weeks. Hours may vary by need.

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