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University of IowaPosted 22 days ago

Clin Trials Rsrch Asst/Data Mg - ICTS Coordinator Core

Full-time
Hybrid
1+ years
Competitive
Posted 22 days ago

The University of Iowa is hiring a Clinical Trials Research Assistant/Data Manager for its Institute for Clinical and Translational Science (ICTS) Coordinator Core. The role supports clinical research protocols and studies, including participant recruitment and consent, regulatory documentation, data reporting, and grant and trial budget tracking.

Posted
22 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
  • Research Regulatory Document Processing
  • Attention to Detail

Required skills

Clinical Practice (GCP)Clinical ResearchEpicI-CTMSICartMicrosoft AccessMicrosoft ExcelMicrosoft OutlookMicrosoft WordPublic Health ResearchREDCapRegulatory Documentation

Full job description

The University of Iowa is hiring a Clinical Trials Research Assistant/Data Manager for its Institute for Clinical and Translational Science (ICTS) Coordinator Core. The role supports clinical research protocols and studies, including participant recruitment and consent, regulatory documentation, data reporting, and grant and trial budget tracking.

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
  • 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
  • Basic (6 months - 1 year) of clinical research experience.
  • Clinical Research
  • Public Health
  • Public Health Research
  • Manuscript Writing
  • REDCap
  • Epic
  • ICart
  • I-CTMS
  • Microsoft Access
  • Data Collection
  • Data Entry
  • Research Regulatory Document Processing
  • Independent Work
  • Time Management
  • Attention to Detail

Benefits

  • Paid vacation
  • Sick leave
  • Health, dental, life and disability insurance options
  • Generous employer contributions into retirement plans
  • Hybrid work: a 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.

Company

  • Public research university
  • Iowa City, Iowa, USA
  • https://clas.uiowa.edu/deos/mailing/february-19-2020/iowa-innovation-challenge
  • Founded in 1847
  • 10001+ employees

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, Epic, I-CTMS, ICart, Microsoft Access, Microsoft Excel, Microsoft Outlook, Microsoft Word, Public Health Research, REDCap, 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

  • 1+ years

Job details

Employment type

Full-time

Seniority level

1+ years

Date posted

Oct 22, 2026

Work mode

Hybrid

Job source

uiowa.referrals.selectminds.com

Company

University of Iowa

Healthcare

Public research university

See all 8 jobs from University of Iowa →
  • Iowa City, Iowa, USA
  • Healthcare
  • 10001+ employees
  • Founded 1847
  • clas.uiowa.edu

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