Clinical Research Coordinator (CRC) – Innovo Research in partnership with The Iowa Clinic

The Iowa Clinic • West Des Moines, IA

14d

About The Position

A day in the life…
Wondering what a day in the life of a Clinical Research Coordinator at Innovo Research might look like?
Start your day by reviewing the study schedule, supplies, and priorities with the research team.
Support investigators by preparing for and executing assigned studies in line with protocol, SOPs, and GCP.
Recruit and screen potential participants, maintain screening logs, and help guide the consent process.
Coordinate and conduct study visits and procedures (vital signs, ECG, sample collection, spirometry, and other protocol-required tasks).
Collect, record, and maintain accurate source documentation and study data—quality and completeness matter.
Monitor participant safety and communicate adverse events/reactions to the Principal Investigator and appropriate medical staff.
Prepare for monitoring visits, audits, and inspections while protecting confidential information and PHI.

Requirements

• Bachelor’s degree in a related field.
• 1–2 years of clinical research experience (or relevant clinical/medical experience with equivalent training).
• Working knowledge of clinical trials, research documentation, and medical terminology.
• Ability to apply GCP/ICH principles and applicable FDA regulations and guidelines for human subject protection.
• Comfort performing clinical procedures as required (e.g., phlebotomy, vital signs; other procedures as assigned).
• Strong written and verbal communication skills and the ability to build effective working relationships.
• Excellent organization, attention to detail, and ability to multi-task and manage competing priorities.
• Proficiency with Microsoft Office and routine office/clinical equipment.

Nice To Haves

• You enjoy a fast-paced clinical environment and can stay calm and effective when priorities shift.
• You take pride in data quality, documentation, and doing things the right way.
• You’re a team player who communicates clearly and likes solving problems alongside others.

Responsibilities

• Review study schedule, supplies, and priorities with the research team.
• Support investigators by preparing for and executing assigned studies in line with protocol, SOPs, and GCP.
• Recruit and screen potential participants, maintain screening logs, and help guide the consent process.
• Coordinate and conduct study visits and procedures (vital signs, ECG, sample collection, spirometry, and other protocol-required tasks).
• Collect, record, and maintain accurate source documentation and study data.
• Monitor participant safety and communicate adverse events/reactions to the Principal Investigator and appropriate medical staff.
• Prepare for monitoring visits, audits, and inspections while protecting confidential information and PHI.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level