Clinical Research Coordinator - Oncology
TapTalent.ai
Date: 13 hours ago
City: Detroit, MI
Contract type: Full time

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