Clinical Research Coordinator - Oncology

We're Hiring: Clinical Research Coordinator – Oncology

We are seeking a detail-oriented and motivated Clinical Research Coordinator to support oncology clinical trials onsite in Detroit, MI. In this role, you will ensure regulatory compliance, coordinate day-to-day study activities, and work closely with patients, clinicians, and research staff to support high-impact cancer research.

Location: Detroit, MI

Role: Clinical Research Coordinator – Oncology

What You’ll Do

• Coordinate and manage daily operations of oncology clinical trials
• Ensure adherence to study protocols and federal regulations (GCP, CFR, IRB)
• Serve as a liaison between research participants, sponsors, and investigators
• Schedule and track study visits, data collection, and specimen management
• Maintain regulatory binders, source documentation, and accurate records
• Assist in subject recruitment, enrollment, and retention strategies
• Monitor patient safety and report adverse events in compliance with protocol
  
  

What We’re Looking For

• Bachelor’s degree in Life Sciences or a related field
• Minimum of 1 year of clinical research experience, preferably in oncology
• Familiarity with IRB submissions, regulatory documentation, and GCP guidelines
• Certification (SOCRA or ACRP) preferred
• Strong attention to detail, organization, and time management skills
• Excellent written and verbal communication abilities
• Proficient in Microsoft Office and clinical trial data systems
  
  

This is an excellent opportunity to contribute to cutting-edge oncology research while growing your clinical research career in a collaborative and mission-driven environment.

Equal opportunity employer. All qualified applicants will receive consideration without regard to race, color, religion, gender, national origin, disability, or veteran status.