Multisite Clinical Research Coordinator II – NCTN Trials

Fred Hutchinson Cancer Center (Fred Hutch); Seattle (WA); On-site; USD 45,000 - 67,000; Full time

Benefits offered by this job

Medical insurance

Vision insurance

Dental insurance

Tuition reimbursement

Paid vacation

Paid sick leave

Paid holidays

Paid parental leave

Retirement plan

Employee assistance program

Onsite health clinic

Job summary

Fred Hutchinson Cancer Center in Seattle seeks a Clinical Research Coordinator II to manage day-to-day operations of NCTN trials, including screening, enrollment, and data handling. You will liaise with investigators and study teams to ensure compliant conduct across multiple disease programs.

Your role requires strong organizational skills, attention to detail, and effective communication to coordinate study logistics, monitor patient visits, and support budget and billing processes within a

Qualifications

• High school diploma or equivalent.
• 2–3 years' clinical research or cancer registry experience.
• Knowledge of clinical trials records, procedures, and data systems.
• Ability to synthesize study conduct.

Responsibilities

• Conduct daily clinical operations of assigned studies per protocols and regulatory guidelines.
• Develop and maintain study tools and reference materials.
• Create and disseminate study education content for internal and external audiences.
• Coordinate patient enrollment by reviewing records for eligibility and obtaining consent.

Skills

Attention to detail

Written communication

Verbal communication

Computer skills

Team collaboration

Problem solving

Organizational skills

Education

High school diploma or equivalent

Associate or bachelor’s degree preferred

CCRC or SOCRA certification preferred

Job description

Fred Hutchinson Cancer Center in Seattle seeks a Clinical Research Coordinator II to manage day-to-day operations of NCTN trials, including screening, enrollment, and data handling. You will liaise with investigators and study teams to ensure compliant conduct across multiple disease programs.

Your role requires strong organizational skills, attention to detail, and effective communication to coordinate study logistics, monitor patient visits, and support budget and billing processes within a