Clinical Trial Site Manager – Oncology (Multi-Site)

University of Kansas Medical Center; United States; On-site; USD 61,000 - 91,000; Full time

Benefits offered by this job

Health, dental, vision insurance

Paid time off and holidays

Retirement benefits

Job summary

The University of Kansas Medical Center Cancer Center is seeking a Clinical Site Manager to oversee all aspects of clinical trial site monitoring, including visits, site initiation, and regulatory documentation. You will ensure GCP compliance and data integrity across investigator-initiated trials.

Responsibilities include RBM/SDV monitoring, data verification, and coordinating with multi-site teams on IIT development and onboarding, with support for audits and regulatory inspections.

Qualifications

• Work Experience: 6 years of relevant work experience.
• Experience with FDA regulations relevant to drugs, devices, biologics.
• Relevant education may substitute for experience.

Responsibilities

• Conduct interim monitoring reviews for investigator-initiated trials.
• Review and verify CRFs, regulatory files, and Trial Master File documentation.
• Ensure informed consent, subject eligibility, and enrollment procedures.
• Coordinate IIT enrollment and multisite development across sites.
• Support external audits and FDA inspection readiness.

Skills

Attention to detail

Problem solving

Multitasking

Interpersonal skills

Organization

Communication

Computer skills

Tools

SmartSheet

REDCap

CRIS/Velos CTMS

Job description

The University of Kansas Medical Center Cancer Center is seeking a Clinical Site Manager to oversee all aspects of clinical trial site monitoring, including visits, site initiation, and regulatory documentation. You will ensure GCP compliance and data integrity across investigator-initiated trials.

Responsibilities include RBM/SDV monitoring, data verification, and coordinating with multi-site teams on IIT development and onboarding, with support for audits and regulatory inspections.