Clinical Trials Data Management Assistant – Onsite

University of Iowa; Iowa City (IA); On-site; USD 52,000 - 68,000; Full time

Job summary

The University of Iowa seeks a Clinical Trials Research Assistant/Data Manager in the Department of Surgery to support recruitment, consent, data collection, and regulatory submissions for clinical studies led by Dr. Vikas Dudeja.

You will develop and maintain study protocols, assist with data systems (REDCap, Epic, ACCESS), and coordinate with clinicians, sponsors, and IRB to ensure compliant trial conduct. This is a full-time on-campus role.

Qualifications

• Bachelor’s degree in Health Science or equivalent required.
• Excellent written and verbal communication skills required.
• Ability to work nights and weekends required.
• Proficiency in Word, Outlook and Excel required.

Responsibilities

• Perform clinical/health care research activities.
• Screen, recruit, enroll and obtain informed consent for clinical research activities.
• Educate patient scope of study, risks/benefits, alternatives, and study requirements.
• Relay information to PI and verify patient eligibility.
• Oversee recruitment of subjects and scheduling of trial procedures.
• Prepare study recruitment materials.
• Assist in design, development, execution, and maintenance of protocols and studies.
• Oversee CRF development and review query reports.
• Monitor data systems and regulatory documentation.
• Prepare regulatory submissions and assist with IRB/ACURF submissions.
• Track grant/trial budgets and identify unspent funds.

Skills

Written communication

Verbal communication

Microsoft Word

Outlook

Excel

Education

Bachelor’s degree in Health Science

Tools

REDCap

Epic

I-CART

ACCESS

Job description

The University of Iowa seeks a Clinical Trials Research Assistant/Data Manager in the Department of Surgery to support recruitment, consent, data collection, and regulatory submissions for clinical studies led by Dr. Vikas Dudeja.

You will develop and maintain study protocols, assist with data systems (REDCap, Epic, ACCESS), and coordinate with clinicians, sponsors, and IRB to ensure compliant trial conduct. This is a full-time on-campus role.