Oncology CRC II: Lead Community Site Trials

Fred Hutch; Seattle (WA); On-site; USD 44,000 - 66,000; Full time

Benefits offered by this job

Medical benefits

Dental benefits

Tuition reimbursement

Paid vacation

Job summary

Fred Hutchinson Cancer Center in Seattle is recruiting a Clinical Research Coordinator II to manage day‑to‑day activities for Phase I–III trials and observational studies across community sites.

You will coordinate screening, enrollment, visits, data collection, and regulatory compliance while collaborating with investigators, sponsors, and clinical teams. Travel between community sites may be required.

Qualifications

• Two to three years’ experience in a clinical research or cancer registry environment with regulatory or human research protections.
• Knowledge of clinical trials records, procedures, and computerized data processing systems.
• Demonstrated knowledge of how to synthesize study conduct.
• Associate or bachelor’s degree preferred; certifications welcomed.

Responsibilities

• Conduct daily clinical operations of assigned research studies per protocol and regulatory standards.
• Support startup, site activation, training, and workflow development.
• Coordinate enrollment, eligibility review, informed consent, and visit scheduling.
• Ensure data entry, source documentation, and regulatory compliance are maintained.
• Collaborate with multiple departments to support protocol implementation and patient care.
• Prepare for sponsor monitoring visits and respond to requests.

Skills

Clinical research experience

Regulatory knowledge

Documentation accuracy

Study conduct synthesis

Education

Associate or bachelor’s degree

CCRC certification (SOCRA)

Job description

Fred Hutchinson Cancer Center in Seattle is recruiting a Clinical Research Coordinator II to manage day‑to‑day activities for Phase I–III trials and observational studies across community sites.

You will coordinate screening, enrollment, visits, data collection, and regulatory compliance while collaborating with investigators, sponsors, and clinical teams. Travel between community sites may be required.