Oncology Clinical Research Monitor II - Remote

Fred Hutch; Seattle (WA); On-site; USD 97,822 - 146,681; Full time

Benefits offered by this job

Medical/vision/dental benefits

Paid vacation (12-22 days per year)

Tuition reimbursement

Job summary

Fred Hutch in Seattle seeks a Clinical Research Monitor II to support quality and regulatory compliance in oncology clinical trials. You will conduct monitoring activities to ensure adherence to protocol and regulatory requirements, working closely with investigators and study teams to ensure data integrity and participant safety.

Ideal candidates will have at least 7 years of clinical research monitoring experience, preferably in oncology, along with in-depth knowledge of FDA regulations and GCP guidelines. Excellent communication and analytical skills are essential for this role.

Qualifications

• Minimum of 7+ years of experience in clinical research monitoring, preferably in oncology.
• Strong knowledge of clinical research with exceptional written, verbal, and interpersonal skills.
• In-depth knowledge of FDA regulations and GCP guidelines.

Responsibilities

• Independently conduct routine and for-cause monitoring of oncology clinical trials.
• Document monitoring observations, prepare reports, and oversee issues.
• Work collaboratively with Principal Investigators to resolve findings.

Skills

Clinical research monitoring

Communication skills

Analytical abilities

Compliance risk identification

Education

Bachelor's or advanced degree

Tools

Electronic data capture (EDC) systems

Job description

Fred Hutch in Seattle seeks a Clinical Research Monitor II to support quality and regulatory compliance in oncology clinical trials. You will conduct monitoring activities to ensure adherence to protocol and regulatory requirements, working closely with investigators and study teams to ensure data integrity and participant safety.

Ideal candidates will have at least 7 years of clinical research monitoring experience, preferably in oncology, along with in-depth knowledge of FDA regulations and GCP guidelines. Excellent communication and analytical skills are essential for this role.