Oncology Clinical Research Associate - Midwest Travel

Regulatory Toolkit; Detroit (MI); On-site; USD 70,000 - 100,000; Full time

Job summary

ICON Strategic Solutions seeks a Clinical Research Associate - Oncology to join our sponsor-dedicated team in Detroit, MI. You will monitor sites, manage trials, and ensure compliance with ICH-GCP, CTMS, and eTMF, while supporting patient safety and data integrity.

Travel up to 50% across the Midwest is required, with preference for candidates near Detroit. The role requires a life sciences degree or RN, 2+ years of on-site monitoring in pharma or CRO, and the ability to work legally in the

Qualifications

• 2+ years of on-site monitoring experience in pharma/CRO
• Experience monitoring oncology clinical trials
• Proficient with ICH-GCP and local regulatory requirements

Responsibilities

• Serve as primary contact between investigational sites and sponsor (Oncology).
• Conduct site visits: selection, initiation, monitoring, close-out.
• Ensure site compliance with ICH-GCP, SOPs, and regulations.
• Maintain CTMS and eTMF documentation.
• Support training and maintain compliance records.
• Monitor patient safety and AE/SAE reporting.
• Support site recruitment and retention.
• Oversee drug accountability and storage/destruction.
• Resolve data queries and ensure timely data entry.
• Escalate risks to the clinical team.
• Track site budgets and payments; collaborate with CTAs, LTMs, CTMs.

Skills

On-site monitoring experience

Communication skills

Travel willingness

Education

Bachelor's degree Life Sciences or equivalent

RN qualification

Tools

CTMS

eTMF

Job description

ICON Strategic Solutions seeks a Clinical Research Associate - Oncology to join our sponsor-dedicated team in Detroit, MI. You will monitor sites, manage trials, and ensure compliance with ICH-GCP, CTMS, and eTMF, while supporting patient safety and data integrity.

Travel up to 50% across the Midwest is required, with preference for candidates near Detroit. The role requires a life sciences degree or RN, 2+ years of on-site monitoring in pharma or CRO, and the ability to work legally in the