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Clinical Trials Jobs in Iowa (NOW HIRING)

CRO Strategies

Clinical Research Coordinator

Des Moines, IA · Remote

$23.75 - $31.50/hr

Proficiency with Clinical Trials processes and conducting them in compliance with guidelines * Strong organizational, communication, and attention-to-detail skills * Ability to work independently in ...

CRO Strategies

Clinical Research Coordinator

Des Moines, IA · Remote

$23.75 - $31.50/hr

Proficiency with Clinical Trials processes and conducting them in compliance with guidelines * Strong organizational, communication, and attention-to-detail skills * Ability to work independently in ...

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$27

$58

$90

How much do clinical trials jobs pay per hour?

As of May 28, 2026, the average hourly pay for clinical trials in Iowa is $58.72, according to ZipRecruiter salary data. Most workers in this role earn between $47.64 and $66.15 per hour, depending on experience, location, and employer.

What is a Clinical Trials job?

A Clinical Trials job involves managing, coordinating, or supporting research studies that evaluate the safety and effectiveness of medical treatments, drugs, or devices. Professionals in this field work on trial design, patient recruitment, data collection, regulatory compliance, and reporting results. Roles can range from clinical research coordinators to trial managers and regulatory specialists. The goal is to ensure that studies follow ethical guidelines and produce reliable data for medical advancements.

What are the key skills and qualifications needed to thrive in the Clinical Trials position, and why are they important?

To thrive in Clinical Trials roles, you need a strong understanding of clinical research principles, Good Clinical Practice (GCP) guidelines, and a background in life sciences or healthcare. Familiarity with electronic data capture (EDC) systems, regulatory compliance software, and relevant certifications such as GCP or CCRA is highly valuable. Attention to detail, organizational skills, and effective communication enable collaboration across multidisciplinary teams. These competencies are crucial for ensuring protocol adherence, data integrity, and the successful execution of trial activities.

What are some common career paths or advancement opportunities for professionals working in Clinical Trials?

Many professionals in Clinical Trials start their careers as Clinical Research Coordinators, Clinical Research Associates, or Data Managers. With experience, you can advance to roles such as Senior Clinical Research Associate, Clinical Trial Manager, or Project Manager, and potentially move into areas like regulatory affairs, medical writing, or quality assurance. The role offers continuous learning opportunities, exposure to innovative therapies, and often provides the chance to lead larger, more complex studies as you progress. Advancement is typically supported by additional certifications, strong performance, and a proactive approach to professional development. Teamwork and networking within the industry can also open new doors for growth.
More about Clinical Trials jobs
What are the most commonly searched types of Clinical Trials jobs in Iowa? The most popular types of Clinical Trials jobs in Iowa are:
What are popular job titles related to Clinical Trials jobs in Iowa? For Clinical Trials jobs in Iowa, the most frequently searched job titles are:
What job categories do people searching Clinical Trials jobs in Iowa look for? The top searched job categories for Clinical Trials jobs in Iowa are:
What cities in Iowa are hiring for Clinical Trials jobs? Cities in Iowa with the most Clinical Trials job openings:
Clinical Trials jobs near you
Infographic showing various Clinical Trials job openings in Iowa as of May 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $122,137 per year, or $58.7 per hour.
Clinical Trials Research Assistant - Pediatric Neurology

Clinical Trials Research Assistant - Pediatric Neurology

University of Iowa Hospitals & Clinics

Iowa City, IA • On-site

$23.75 - $31.50/hr

Full-time

Posted 9 days ago

Job description

Description
To manage and support clinical trial regulatory activities for the Pediatric Department, Clinical Research Services. Act as back-up study coordinator for studies as appropriate.
This is a specified term position.
Duties to include:
  • Take primary responsibility in collaboration with study lead coordinator to complete regulatory activities to open new clinical trials.
  • Serve as a resource and support to study coordinators for regulatory activities required to maintain and close clinical trials.
  • Coordinate specific aspects of external review and internal processes. Specifically, oversee the preparation and submission of the appropriate Human Subjects Review forms and application materials to the Institutional Review Board (IRB-01), and central IRB entities. Collaborate with study-specific coordinator to prepare consent forms for research protocols and local and central IRB submissions.
  • Prepare and submit application forms and serve as liaison to the Clinical Research Unit (CRU), the Pharmacy and Therapeutics Committee, the Medical Radiation Protection Committee, the Protocol Review and Monitoring Committee, Joint Office of Compliance, Nursing Research Committee, Pathology Committee, and other review committees as necessary.
  • Support the primary study coordinator(s) as needed on additional regulatory tasks (such as annual reviews, modifications, Adverse Events, Safety Reports and other reportable events to IRB).
  • Coordinate the regulatory process and document preparation used in the implementation of clinical trials.
  • Serve as liaison to clinicians, research investigators, data managers, nursing services staff, pharmacists and medical personnel to ensure sufficient cooperation among participating stakeholders for each clinical research study. Assist in the execution, administration and maintenance of protocols and clinical studies. Provide input into descriptions of research procedures.
  • Coordinate specific aspects of external review and align with internal processes. Manage and organize regulatory documentation from sites and regulatory authorities. Prepare regulatory submissions and assist with on-site audits when needed.
  • Monitor compliance with regulatory guidelines and ensure proper maintenance of documents. Work with primary coordinator to develop regulatory files and binders, assist as requested in maintenance.
  • Assist primary study coordinator(s) with monitoring and auditing issues that relate to regulatory activities, when needed.
  • Enter data for the evaluation of clinical research metrics through our OnCore database as it relates to the initial regulatory review and submission process.
  • Assist study staff with compliance of policies and procedures as they relate to regulatory activities.
  • Prepare and deliver basic content that enhances knowledge of and compliance with internal and external standards and regulations.
  • Attend all appropriate meetings as assigned: this will include but is not limited to with internal and external groups to provide reporting of study updates, educational and training meetings, meetings with team leads and supervisors, and meetings with sponsors or CROs.
  • Assist in general coordinator activities as required as a back-up coordinator. These might include study-specific training, assist with preparing for and completing subject visits, data entry, and other study specific tasks as appropriate.

Qualifications
Education Requirements
  • A Bachelor's Degree or an equivalent combination of education and experience

Required Qualifications
  • Excellent written, verbal and interpersonal communication skills
  • Excellent organizational and time management skills
  • Proficient in computer software applications including spreadsheet and database experience
  • Experience in coordinating multiple projects and various functions independently
  • Prior experience with Institutional Review Board application materials and processing
  • Knowledge of regulations that apply to human research
  • Proven ability to utilize medical terminology

Desired Qualifications
  • Experience working in a research facility with protocols or management of clinical data, i.e., laboratory values, toxicity levels
  • 1-3 years administrative and/or program management experience
  • Knowledge of University of Iowa policies, procedures and regulations

Position and Application details:
In order to be considered for an interview, applicants must upload the following documents and mark them as a "Relevant File" to the submission:
  • Resume
  • Cover Letter

Job openings are posted for a minimum of 7 calendar days and may be removed from posting and filled any time after the original posting period has ended.
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 pedsuichildrenshr@healthcare.uiowa.edu
This position is not eligible for University sponsorship for employment authorization.

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