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Clinical Trial Associate Jobs in Iowa (NOW HIRING)

410 ICR United States USA

Senior CRA

Ames, IA · On-site

Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements. * Proven ability to manage multiple sites and projects ...

Iterative Health

Clinical Research Coordinator II

Waterloo, IA · On-site

$22.50 - $30/hr

By combining deep clinical trial expertise with cutting-edge AI, we connect sponsors' scientific ... Associate's or Bachelor's degree in a scientific, healthcare, or related discipline required * 3-5 ...

Iterative Health

Clinical Research Coordinator II

Waterloo, IA · On-site

$24 - $31.75/hr

By combining deep clinical trial expertise with cutting-edge AI, we connect sponsors' scientific ... Associate's or Bachelor's degree in a scientific, healthcare, or related discipline required * 3-5 ...

University of Iowa

NEUROENDOCRINE ONCOLOGIST

Iowa City, IA · On-site

$193/hr

This position will be at the rank of Assistant Professor, Associate Professor or Full Professor to ... Nationally or internationally recognized clinical trial experience. * Academic experience with ...

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How much do clinical trial associate jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for clinical trial associate in Iowa is $37.56, according to ZipRecruiter salary data. Most workers in this role earn between $30.24 and $41.30 per hour, depending on experience, location, and employer.

What is a clinical trial associate?

A clinical trial associate helps oversee late-stage drug trials. They design and implement the final clinical study before making reports to the FDA and other regulatory bodies. Their duties cover logistics, including ordering supplies, auditing all reports and documents, and ensuring their timely completion. They are responsible for making sure that the trial follows all ICH and GCP requirements.

What does a clinical trial associate do?

A Clinical Trial Associate (CTA) is responsible for supporting the planning, coordination, and management of clinical trials. They help ensure studies comply with regulatory requirements and assist in maintaining trial documentation, tracking study progress, and communicating with clinical sites. CTAs work closely with clinical research teams, sponsors, and vendors to keep trials running smoothly and efficiently. Their administrative and logistical support is essential for successful clinical research.

What are the key skills and qualifications needed to thrive as a clinical trial associate?

To thrive as a Clinical Trial Associate, you need a solid understanding of clinical research processes, regulatory guidelines, and a relevant life sciences degree. Familiarity with electronic data capture (EDC) systems, CTMS (Clinical Trial Management Systems), and GCP (Good Clinical Practice) certification are commonly required. Attention to detail, strong organizational skills, and effective communication set top performers apart in this role. These competencies are crucial for ensuring compliance, accurate data management, and smooth coordination of clinical trial activities.

What are some common challenges faced by clinical trial associates when managing study documentation?

Clinical Trial Associates often encounter challenges related to maintaining accurate and up-to-date trial documentation, as protocols and regulatory requirements can change frequently. Ensuring all documents are correctly filed, version-controlled, and accessible for audits requires strong attention to detail and organizational skills. Additionally, coordinating with multiple stakeholders—such as clinical research coordinators, data managers, and regulatory teams—can add complexity to document management. Proactive communication and adopting robust documentation systems can help overcome these challenges.

What is the difference between Clinical Trial Associate vs Clinical Research Coordinator?

AspectClinical Trial AssociateClinical Research Coordinator
CredentialsBachelor's degree, often in life sciences; certifications like ACRP or SOCRABachelor's degree in health sciences or related field; similar certifications
Work EnvironmentPharmaceutical companies, CROs, clinical trial sitesHospital, academic medical centers, clinical trial sites
ResponsibilitiesAssist in trial setup, data collection, regulatory complianceManage patient recruitment, conduct visits, data entry
Industry UsageCommon in pharmaceutical and biotech industriesCommon in hospitals and academic research settings

Both roles support clinical trials but differ mainly in scope and setting. Clinical Trial Associates typically work in industry settings focusing on trial logistics and compliance, while Clinical Research Coordinators often manage patient interactions and data at clinical sites. Understanding these differences helps in choosing the right career path or job search focus.

More about Clinical Trial Associate jobs

What are the most commonly searched types of Clinical Trial jobs in Iowa?

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Clinical Trial Associate jobs near you
Infographic showing various Clinical Trial Associate job openings in Iowa as of August 2026, with employment types broken down into 2% As Needed, 69% Full Time, 27% Part Time, 1% Temporary, and 1% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $78,118 per year, or $37.6 per hour.

100% Clinical Trial & Data Management Research Associate - Emergency Medicine

The University Of Iowa

Iowa City, IA

$32.75 - $44.75/hr

Full-time

Posted 13 days ago

University Of Iowa rating

6.9

Company rating: 6.9 out of 10

Based on 85 frontline employees who took The Breakroom Quiz

462nd of 620 rated colleges and universities

Job description

The Clinical Trial & Data Management Research Associate role in Emergency Medicine (EM) will be an integral member of the research team. This position will provide support for Emergency Medicine working alongside the ICTS team performing activities which are vitally important to grow and foster innovation through research support endeavors. This position will apply clinical skills to administer, deliver, and evaluate research protocols.

Research/Clinical Activities, Subject Recruitment and Enrollment

  • Screen participant for study eligibility. 

  • Educate participant on scope of study, potential risks and benefits, possible alternatives, and study requirements for participant. 

  • Communicate with principal investigator and verify participant eligibility. 

  • Administer study treatments and identify adverse reactions. 

  • Recruit, enroll and obtain informed consent for clinical research activities. Oversee the recruitment of participants and scheduling of trial-related procedures. 

  • Prepare study recruitment materials. Develop complex study recruitment materials. 

Protocol Development/Management and Study Responsibilities

  • Collaborate with Principal Investigator and the study team in the development, execution, administration and maintenance of protocols and clinical studies and provide input into descriptions of complex research procedures. 

  • Assess participants for problems related to protocol. Oversee CRF development, database development and maintenance. 

  • Review query reports. Resolve all monitoring visit issues. 

  • Perform and monitor randomizations. 

  • Develop complex study materials used in conduction of study. 

  • Communicate with local health care practitioners, agencies, and sponsors as needed. 

Data Collection and Monitoring

  • Participate in the design, development, and testing of clinical research trial data systems. 

  • Maintain communication between health care clinical information systems and research data systems. 

  • Collect and validate data.  Make recommendations for query resolution. 

  • Assist with identification of data problems and implement change as needed. 

Regulatory Guidelines and Documents

  • Manage and organize regulatory documentation. 

  • Prepare and submit regulatory documents. 

  • Assist sponsor with on-site audits of research and clinical data. 

  • Monitor and maintain compliance of regulatory guidelines and documents. 

  • Prepare and present Institutional Review Boards or other submissions and required regulatory documents. 

  • Carry out corrective action plan for reportable events.

Financial Responsibility

  • Assist in the development and administer study budgets. 

  • Participate in preparation of grant applications for extramural funding. 

  • Oversee internal pilot funding program application process. 

  • Assist with tracking and reconciling grant budget free balances and identify opportunities to ensure that grant funding is being used as intended and awarded.

Education Requirements: A Bachelor's degree in a Health Science field or an equivalent combination of education and research experience.:

  • A Bachelor's degree in a Health Science field or an equivalent combination of education and research experience. 

Experience Requirements: 

  • A minimum of one year experience designing, developing, and implementing recruitment program materials. 

  • Working knowledge of Good Clinical Practice (GCP) in research. 

  • Excellent written and verbal communication skills. 

  • Ability to work nights and weekends. 

  • Must be proficient in computer software applications (MS Word, Excel, PowerPoint, and Outlook).

Desired Qualifications:

  • Experience with REDCap, Epic and ACCESS. 

  • Previous experience in data collection and entry. 

  • Experience in processing research regulatory documents and ethics preparation. 

  • Excellent time management skills and ability to perform detail oriented work. 

  • 1-3 years of clinical research experience. 

  • Experience developing and working with research budgets/billing. 

  • A current, valid Registered Nurse license or Respiratory Therapist license. 

  • Database management experience including entering, tracking and maintaining data and troubleshooting 

Application Process:  In order to be considered, applications must upload a resume. Job openings are posted for a minimum of 7 calendar days. This job may be removed from posting and filled any time after the minimum posting period has ended. For questions or additional information, please contact Katie McVay at katie-mcvay@uiowa.edu. 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. 

Additional Information
  • Classification Title: Clin Trials Rsrch Associate
  • Appointment Type: Professional and Scientific
  • Schedule: Full-time
  • Work Modality Options: On Campus
Compensation
  • Pay Level: 4A
Contact Information
  • Organization: Healthcare
  • Contact Name: Katie McVay
  • Contact Email: katie-mcvay@uiowa.edu

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