Multi-Site Oncology Clinical Trials Coordinator

Oncology Voice Network LLC

Illinois

Hybrid

USD 87,968,000 - 131,952,000

Full time

4 days ago
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Benefits offered by this job

Health insurance
Dental insurance
Paid time off

Job summary

Advocate Health in Illinois seeks a Clinical Research Coordinator to oversee multi-site trials, ensuring start-up, IRB submissions, recruitment, and data integrity. You will coordinate investigators, sponsors, and clinical staff to maintain high-quality research conduct.

You will mentor team members, develop educational plans, and ensure EMR and lab procedures meet protocol requirements. This role supports physicians and nurses within a structured research program.

Qualifications

  • Bachelor's degree in Biology, Health Science, Nursing, or related field.
  • Typically requires 2 years of experience in Research.
  • Knowledge of GCP, ICH, FDA Guidance, and DHHS regulations.

Responsibilities

  • Coordinate sponsored clinical trials across sites, including start-up, CTA/budget/CTMS reviews, IRB submissions, recruitment, and enrollment.
  • Serve as liaison between sponsor and investigators and primary contact for study team.
  • Develop educational plans to disseminate protocol information and train staff.
  • Ensure specimen procurement, processing, and shipment meet lab requirements.
  • Guide and mentor research team; oversee training and competency in research applications.

Skills

Good Clinical Practices
ICH Guidelines
Verbal and written communication
Mentoring team members
EMR proficiency

Education

Bachelor's Degree in Biology
Bachelor's Degree in Health Science
Bachelor's Degree in Nursing

Tools

EMR
Microsoft Office Suite

Job description

Advocate Health in Illinois seeks a Clinical Research Coordinator to oversee multi-site trials, ensuring start-up, IRB submissions, recruitment, and data integrity. You will coordinate investigators, sponsors, and clinical staff to maintain high-quality research conduct.

You will mentor team members, develop educational plans, and ensure EMR and lab procedures meet protocol requirements. This role supports physicians and nurses within a structured research program.

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