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University of Iowa ResearchPosted 23 days ago

Clin Trials Rsrch Asst/Data Mg - ICTS Coordinator Core

Full-time
Hybrid
Entry level
Competitive
Posted 23 days ago

The University of Iowa is hiring a Clinical Trials Research Assistant/Data Manager for the ICTS Coordinator Core. The role supports clinical and health care research by administering research protocols, coordinating participant recruitment and consent, managing regulatory documentation and data, and assisting with grant and trial budgets.

Research

Posted
23 days ago
Source
uiowa.referrals.selectminds.com
Sector
Healthcare

Opens the employer's application page in a new tab

Responsibilities

  • Perform clinical/health care research activities in various departments
  • Screen, recruit, enroll and obtain informed consent for clinical research activities
  • Assist in the design, development, execution, administration and maintenance of protocols and clinical studies and provide input into descriptions of complex research procedures
  • Assist patients with problems related to protocol
  • Manage and organize regulatory documentation
  • Prepare regulatory submissions
  • Conduct literature reviews and maintain citation database
  • Pull data reports from qualitative data management software
  • Participate in preparation of grant applications for extramural funding
  • Provide assistance with tracking and reconciling grant/trial budget free balances and identify opportunities to ensure that grant funding is being used as intended and awarded

Qualifications

  • A Bachelor's degree in a Health Science field or an equivalent combination of education and research experience
  • Excellent written and verbal communication skills
  • Working knowledge of Good Clinical Practice (GCP) in research
  • Proficiency in Microsoft Word, Outlook and Excel
  • This position is not eligible for University sponsorship for employment authorization

Preferred

  • Basic (6 months - 1 year) of clinical research experience
  • Educational background in public health or experience participating in public health research projects
  • Previous experience writing manuscripts for publication
  • Experience with REDCap, Epic, ICart, I-CTMS, and ACCESS
  • Previous experience in data collection and entry
  • Experience in processing research regulatory documents
  • The ability to work independently
  • Excellent time management skills and ability to perform detail-oriented work

Required skills

Clinical Practice (GCP)Clinical ResearchData Collection and EntryEpicI-CTMSICartManuscript WritingMicrosoft AccessMicrosoft ExcelMicrosoft OutlookMicrosoft WordPublic Health ResearchREDCapResearch Regulatory Documentation

Full job description

The University of Iowa is hiring a Clinical Trials Research Assistant/Data Manager for the ICTS Coordinator Core. The role supports clinical and health care research by administering research protocols, coordinating participant recruitment and consent, managing regulatory documentation and data, and assisting with grant and trial budgets.

Research

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Responsibilities

  • Perform clinical/health care research activities in various departments
  • Screen, recruit, enroll and obtain informed consent for clinical research activities
  • Assist in the design, development, execution, administration and maintenance of protocols and clinical studies and provide input into descriptions of complex research procedures
  • Assist patients with problems related to protocol
  • Manage and organize regulatory documentation
  • Prepare regulatory submissions
  • Conduct literature reviews and maintain citation database
  • Pull data reports from qualitative data management software
  • Participate in preparation of grant applications for extramural funding
  • Provide assistance with tracking and reconciling grant/trial budget free balances and identify opportunities to ensure that grant funding is being used as intended and awarded

Preferred

  • Basic (6 months - 1 year) of clinical research experience
  • Educational background in public health or experience participating in public health research projects
  • Previous experience writing manuscripts for publication
  • Experience with REDCap, Epic, ICart, I-CTMS, and ACCESS
  • Previous experience in data collection and entry
  • Experience in processing research regulatory documents
  • The ability to work independently
  • Excellent time management skills and ability to perform detail-oriented work

Benefits

  • Paid vacation
  • Sick leave
  • Health, dental, life and disability insurance options
  • Generous employer contributions into retirement plans
  • Hybrid within Iowa: combination of on-campus and remote work; remote work must be performed at a location within the state of Iowa and comply with the remote work program and related policies
  • The Office of the Vice President for Research is committed to forging new frontiers of discovery by providing resources and support to researchers and innovators at the University of Iowa, to promote a culture of creativity that enriches the campus, the state, and the world.
  • Iowa City, Iowa, US
  • https://research.uiowa.edu
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Qualifications

  • A Bachelor's degree in a Health Science field or an equivalent combination of education and research experience
  • Excellent written and verbal communication skills
  • Working knowledge of Good Clinical Practice (GCP) in research
  • Proficiency in Microsoft Word, Outlook and Excel
  • This position is not eligible for University sponsorship for employment authorization
  • Basic (6 months - 1 year) of clinical research experience
  • Educational background in public health or experience participating in public health research projects
  • Previous experience writing manuscripts for publication
  • Experience with REDCap, Epic, ICart, I-CTMS, and ACCESS
  • Previous experience in data collection and entry
  • Experience in processing research regulatory documents
  • The ability to work independently
  • Excellent time management skills and ability to perform detail-oriented work

Required skills

  • Clinical Practice (GCP), Clinical Research, Data Collection and Entry, Epic, I-CTMS, ICart, Manuscript Writing, Microsoft Access, Microsoft Excel, Microsoft Outlook, Microsoft Word, Public Health Research, REDCap, Research Regulatory Documentation

Preferred skills

  • Basic (6 months - 1 year) of clinical research experience, Experience in processing research regulatory documents, Experience with REDCap, Epic, ICart, I-CTMS, and ACCESS, Previous experience in data collection and entry, Previous experience writing manuscripts for publication, The ability to work independently

Experience

  • Entry level

Job details

Employment type

Full-time

Seniority level

Entry level

Date posted

Oct 21, 2026

Work mode

Hybrid

Job source

uiowa.referrals.selectminds.com

Company

University of Iowa Research

Healthcare

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  • Iowa City, IA
  • Healthcare

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