Clinical Research Assistant (CRA) – Innovo Research in partnership with The Iowa Clinic

A day in the life…

Wondering what a day in the life of a Clinical Research Assistant at Innovo Research might look like?

• Coordinate key study activities—from start-up to close-out—by staying organized, responsive, and protocol-focused.
• Support providers and study representatives as a liaison, helping keep communication clear across the research team and patients.
• Recruit, screen, and schedule prospective participants using medical records, databases, referrals, and community outreach.
• Help guide the informed consent process (as delegated and required) and document interactions according to protocol and regulatory standards.
• Support study visits by collecting medical information, performing or arranging phlebotomy, and preparing/handling labs for shipment and review.
• Maintain accurate study documentation (source, case report forms, and regulatory files) and keep supplies stocked for protocol needs.
• Prepare for monitor visits and support ongoing regulatory compliance while protecting patient privacy and confidentiality.
  
  

This job might be for you if you have…

Qualifications

• High school diploma or equivalent (Bachelor’s degree preferred).
• Experience in a clinical setting (2–5 years a plus), with comfort working directly with patients.
• Strong organization, attention to detail, and ability to maintain accurate records and documentation.
• Clear written and verbal communication skills and the ability to work effectively with providers, sponsors/monitors, and internal teams.
• Comfort using computers, email, and standard office/clinical systems (EMR and scheduling experience a plus).
• Commitment to confidentiality and ethical conduct in a clinical research environment (GCP and FDA/OSHA knowledge a plus).
  
  

Bonus points if…

• You have phlebotomy experience or certification and are comfortable with sample handling/shipping.
• You have CNA/medical assistant training or similar hands-on clinical education.
• You enjoy a fast-paced clinic environment, stay calm when priorities change, and take pride in quality documentation.
  
  

This role is in-person at a site-specific clinic location; standard schedule is 40 hours/week, with occasional evenings/weekends as needed.