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  1. Home
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  5. Clinical Trials Research Associate
University of Iowa Research logo

Clinical Trials Research Associate

Not Disclosed•TemporaryHybrid

location_on10, South Gilbert Street, Iowa City, Johnson County, Iowa, 52240, United States

Apply Now

About the Department of Pediatrics

The Stead Family Department of Pediatrics is a national leader in pediatric medicine. Our mission is to provide outstanding care to the children of Iowa and beyond by being a leader in state-of-the-art clinical care, performing cutting-edge research to find new treatments and cures for childhood illnesses, and educating the next generation of pediatric health care providers. The Department comprises the medical and research staff of the UI Stead Family Children’s Hospital, one of the nation’s top-ranked pediatric care and research institutions and Iowa’s only comprehensive children’s hospital.

About the Role

The UI Stead Family Department of Pediatrics, specifically the Hematology/Oncology division, is seeking a full-time Clinical Trials Research Associate (PRV2) to serve as a vital member of the Pediatric Oncology Research Team. This role is designed to coordinate pediatric clinical study activities within the Holden Comprehensive Cancer Center (HCCC) and Stead Family Children’s Hospital at The University of Iowa.

In this position, you will work closely with Clinical Research Coordinators, multiple departments, and the University Clinical Trials Office to plan, deliver, and evaluate healthcare provided to research protocol patients. Your day-to-day work involves managing data entry and electronic data systems, maintaining medical documentation, and ensuring compliance with Institutional Review Board (IRB) requirements. You will act as a liaison to local physicians and hospitals to facilitate care for protocol patients, coordinate ongoing research collaborations with outside institutions, and lead weekly meetings to update the research team on study status and brainstorm solutions to emerging issues.

Note: This position is a Specified Term appointment.

Hiring Process & Application Instructions

To be considered for an interview, applicants must upload the following documents and mark them as a "Relevant File" during submission:

  • Resume
  • Cover Letter

Job openings are posted for a minimum of 7 calendar days and may be removed from posting and filled at any time after the original posting period ends. Successful candidates will be required to self-disclose any conviction history and will be subject to a criminal background check and credential/education verification. Up to 5 professional references will be requested at a later step in the recruitment process.

For additional questions, please contact Bradley at Pedsuichildrenshr@healthcare.uiowa.edu.

Work Arrangement & Eligibility

This position is eligible for a combination of on-campus and remote work. Remote work must be performed within Iowa and will require a work arrangement form to be completed upon the start of your employment. Per policy, work arrangements will be reviewed annually and must comply with the remote work program, related policies, and employee travel policy when working at a remote location.

Please note that this position is not eligible for university sponsorship for employment authorization.

Equal Opportunity Employer

The University of Iowa is an Equal Opportunity/Affirmative Action Employer. We are committed to building a diverse and inclusive community and consider qualified applicants regardless of background, race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.

Work location

Work model: Hybrid

location_on

10, South Gilbert Street, Iowa City, Johnson County, Iowa, 52240, United States

Iowa City, Iowa

Key Responsibilities

  • check_circleCoordinate pediatric clinical study activities and patient care delivery
  • check_circleManage data entry and maintain electronic databases for research protocols
  • check_circleMonitor compliance and maintain documentation for pharmaceutical and in-house trials
  • check_circleProcess and ship biological specimens for laboratory investigations
  • check_circleTrain faculty and staff on good clinical practices and research regulations
  • check_circleServe as liaison to external hospitals to facilitate care for protocol patients
  • check_circleLead weekly team meetings to update study status and resolve issues
  • check_circlePerform statistical analysis and interpret data to support study revisions
  • check_circleCoordinate research collaborations with outside institutions to ensure data consistency

Requirements

  • verifiedBachelor's degree or equivalent combination of education and experience
  • verifiedMinimum 1 year of clinical research experience or medical research data management experience
  • verifiedProficient in Microsoft applications
  • verifiedClinical Research Coordinator Certification (SOCRA or ACRP) preferred
  • verifiedMust upload Resume and Cover Letter
  • verifiedNot eligible for university sponsorship for employment authorization

Nice to Have

Relevant experience in the conduct of both clinical and laboratory oncology research studies. Knowledge of regulatory guidelines and procedures. Experience with pediatrics patient population. Clinical Research Coordinator Certification (SOCRA or ACRP). Knowledge of University of Iowa policies, procedures and regulations.

University of Iowa Research logo
Company

University of Iowa Research

Industry

scientific & qa

View company profilearrow_forwardlanguageWebsite
Quick Overview

Experience

1+ yrs (Entry Level)

Education

Bachelor's degree or equivalent combination of education and experience

Job Type

Temporary

Skills Required

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Skills, education and keywords

Skills: Microsoft Applications, Clinical Research Coordinator Certification, Socra, Acrp, Good Clinical Practices.

Education: Bachelor's degree or equivalent combination of education and experience.

Frequently asked questions about Clinical Trials Research Associate at University of Iowa Research

What does a Clinical Trials Research Associate at University of Iowa Research do?expand_more
In this Clinical Trials Research Associate at University of Iowa Research role, you will coordinate pediatric clinical study activities and patient care delivery; manage data entry and maintain electronic databases for research protocols; monitor compliance and maintain documentation for pharmaceutical and in-house trials; and process and ship biological specimens for laboratory investigations.
What are the requirements for this Clinical Trials Research Associate role?expand_more
To qualify for the Clinical Trials Research Associate at University of Iowa Research position, applicants should have: Bachelor's degree or equivalent combination of education and experience; Minimum 1 year of clinical research experience or medical research data management experience; Proficient in Microsoft applications; Clinical Research Coordinator Certification (SOCRA or ACRP) preferred; Must upload Resume and Cover Letter; and Not eligible for university sponsorship for employment authorization.
Where is the Clinical Trials Research Associate role at University of Iowa Research located?expand_more
Clinical Trials Research Associate at University of Iowa Research is based in 10, South Gilbert Street, Iowa City, Johnson County, Iowa, 52240, United States. This is a hybrid role.
Is this Clinical Trials Research Associate job remote, hybrid, or on-site?expand_more
University of Iowa Research has listed this Clinical Trials Research Associate role as hybrid.
How much experience is required for this Clinical Trials Research Associate role?expand_more
Clinical Trials Research Associate at University of Iowa Research typically requires 1+ years of relevant experience at the entry level level.
What skills do you need for the Clinical Trials Research Associate role at University of Iowa Research?expand_more
Key skills for Clinical Trials Research Associate at University of Iowa Research include Microsoft Applications; Clinical Research Coordinator Certification; Socra; Acrp; and Good Clinical Practices.
What education is required for Clinical Trials Research Associate at University of Iowa Research?expand_more
Educational requirements for this role: Bachelor's degree or equivalent combination of education and experience.
What category does the Clinical Trials Research Associate role belong to?expand_more
Clinical Trials Research Associate at University of Iowa Research is part of the scientific & qa job category on Recrutus.
Recrutus

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check_circle
Collect and verify patient data from charts, lab reports, and source documentation
  • check_circleRecruit, schedule, and coordinate subject participation for clinical trials
  • check_circlePrepare periodic reports for IRB, study sponsors, and principal investigators
  • Microsoft ApplicationsClinical Research Coordinator CertificationSocraAcrpGood Clinical Practices
    US privacy notice
    Accessibility