Clinical Research Coordinator I — Oncology Trials (Hybrid/Remote)

Fred Hutchinson Cancer Research Center; Northern (KY); Hybrid; USD 37,000 - 52,000; Full time

Benefits offered by this job

Medical/vision

Dental

Flexible spending accounts

Life insurance

Disability insurance

Retirement plan

Family life support

Employee assistance program

Onsite health clinic

Tuition reimbursement

Paid vacation

Paid sick leave

Paid holidays

Paid parental leave

Job summary

Fred Hutchinson Cancer Center is seeking a Clinical Research Coordinator I to organize day-to-day operations of hematopoietic cell transplantation observational studies, with a focus on survivorship. You will screen patients, track visits, coordinate procedures, and ensure data quality in line with IRB-approved protocols.

The role reports to Principal Investigators and requires independence within study guidelines.

Qualifications

• High school diploma or equivalent.
• Minimum one year experience in a clinical research or cancer registry environment with regulatory or human research protections.
• Demonstrated knowledge of how to synthesis study conduct.
• Ability to apply judgement in interpreting regulations, determining impacts, and knowing when to elevate questions and concerns when appropriate.

Responsibilities

• Serve as designee of the Principal Investigator to manage daily clinical operations of assigned research studies in accordance with regulatory, GCP guidelines and institutional policy.
• Assist the Principal Investigator with scheduling and taking minutes during conference calls and creating reports.
• Abstract charts to collect study data and enter data into study databases.
• Develop and maintain tools for study implementation, which may include data collection tools and study materials.

Skills

Organizational skills

Communication skills

Education

High school diploma

Bachelor’s degree

Job description

Fred Hutchinson Cancer Center is seeking a Clinical Research Coordinator I to organize day-to-day operations of hematopoietic cell transplantation observational studies, with a focus on survivorship. You will screen patients, track visits, coordinate procedures, and ensure data quality in line with IRB-approved protocols.

The role reports to Principal Investigators and requires independence within study guidelines.