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Clinical Trials Associate Jobs in Iowa (NOW HIRING)

CVAUSA

Clinical Research Coordinator

Davenport, IA · On-site

$55 - $75/hr

Cardiovascular Associates of America (CVAUSA) is a rapidly growing leader in cardiovascular care ... Oversee all aspects of clinical trials, including patient recruitment, screening, and enrollment.

Innovo Research

Clinical Research Nurse

Dubuque, IA · On-site

Manage multiple concurrent trials - screening, recruiting, and enrollment, perform patient/research ... Associate Degree in Nursing from an accredited school of nursing. * Certification in Clinical ...

INNOVO RESEARCH INC

Clinical Research Nurse

Dubuque, IA · On-site

Manage multiple concurrent trials - screening, recruiting, and enrollment, perform patient/research ... Associate Degree in Nursing from an accredited school of nursing. * Certification in Clinical ...

Iterative Health

Clinical Research Coordinator II

Waterloo, IA · On-site

$24 - $31.75/hr

Independently coordinate and manage industry-sponsored clinical trials from study start-up through ... Associate's or Bachelor's degree in a scientific, healthcare, or related discipline required * 3-5 ...

Elanco

Consultant- Clinical Operations

Fort Dodge, IA · Hybrid

Senior Clinical Research Associate (CRA) - Animal Health As a Senior Clinical Research Associate ... Lead the monitoring and execution of farm and companion animal clinical trials, providing oversight ...

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How much do clinical trials associate jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for clinical trials 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 trials associate?

Clinical Trials Associates (CTAs) are professionals who support the planning, coordination, and administration of clinical research studies, often working under the supervision of Clinical Research Coordinators or Managers. Their responsibilities typically include maintaining study documentation, ensuring regulatory compliance, assisting with data collection, and communicating with study sites. CTAs play a critical role in ensuring that clinical trials run smoothly and adhere to strict protocols and guidelines. Their work helps bring new medical treatments and therapies to market safely and efficiently.

What are the key skills and qualifications needed to thrive as a clinical trials associate, and why are they important?

To thrive as a Clinical Trials Associate, you need a solid understanding of clinical research protocols, regulatory compliance, and data management, typically supported by a life sciences degree. Familiarity with systems such as electronic data capture (EDC), clinical trial management systems (CTMS), and knowledge of Good Clinical Practice (GCP) guidelines or related certifications is important. Strong organizational skills, attention to detail, and effective communication help you excel in coordinating study activities and collaborating with diverse teams. These skills ensure accurate trial execution, regulatory adherence, and successful study outcomes.

What are some common challenges faced by clinical trials associates, and how can they be managed effectively?

Clinical Trials Associates often face challenges such as coordinating with multiple stakeholders, managing tight deadlines, and ensuring strict compliance with regulatory guidelines. Balancing administrative tasks with participant communication requires strong organizational skills and attention to detail. Staying proactive in communication, utilizing project management tools, and seeking guidance from senior team members can help manage these challenges effectively while fostering a collaborative team environment.

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

AspectClinical Trials AssociateClinical Research Coordinator
CredentialsBachelor's degree, often in life sciences; certifications like ACRP or SOCRA are commonBachelor's degree in health sciences or related field; certifications like CCRP are advantageous
Work EnvironmentTypically works in clinical trial sites, pharmaceutical companies, or CROsWorks directly at clinical sites, hospitals, or research centers
Job FocusSupports trial setup, data entry, and regulatory complianceManages patient recruitment, scheduling, and data collection

While both roles support clinical research, Clinical Trials Associates primarily focus on trial logistics and compliance, whereas Clinical Research Coordinators handle patient interactions and site management. Both positions require similar educational backgrounds and certifications, often working in the same environments, but their daily responsibilities differ.

Is a clinical trials associate a good career?

A clinical trials associate is a valuable role in the healthcare and pharmaceutical industries, responsible for coordinating and monitoring clinical trial activities. It offers opportunities for career growth, requires attention to detail, and often involves working with regulatory guidelines and data management tools. The role can be stable and rewarding for those interested in medical research and patient safety.

What do I need to be a clinical trials associate?

To become a clinical trials associate, candidates typically need a bachelor's degree in life sciences, healthcare, or a related field. Relevant skills include knowledge of Good Clinical Practice (GCP), attention to detail, and experience with clinical trial management systems or regulatory documentation. Certifications such as the Certified Clinical Research Professional (CCRP) can enhance job prospects.

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 cities in Iowa are hiring for Clinical Trials Associate jobs?

Cities in Iowa with the most Clinical Trials Associate job openings:

Clinical Trials Associate jobs near you
Infographic showing various Clinical Trials Associate job openings in Iowa as of August 2026, with employment types broken down into 2% As Needed, 73% Full Time, 19% Part Time, and 6% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $78,118 per year, or $37.6 per hour.

Clinical Trials Research Assistant/Associate - Pediatric Medical Genetics

University of Iowa

Iowa City, IA • On-site

$47K - $79K/yr

Full-time

Posted 4 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

464th of 629 rated colleges and universities

Job description

The Stead Family Department of Pediatrics, Division of Medical Genetics, is seeking to hire a Clinical Trials Research Assistant or a Clinical Trials Research Associate to manage and coordinate clinical trials related to lysosomal storage disorders and other medical genetic disorders. This is a Specified Term position. This position is not eligible for university sponsorship for employment authorization.
Duties include:
  • Assist with clinical and data coordination for research activities.
  • Screen, recruit, enroll and obtain informed consent for clinical trials.
  • Assist the PI in the completion of regulatory submission and close-out processes.
  • Track study participant data, study drugs, biological specimens, and study procedures.
  • Maintain and disseminate a list of open protocols and informed consents.
  • Prepare regulatory documents for sponsor approval.
  • Consult with researchers to assist in developing a data management plan; design forms to facilitate the collection. Design and coordinate field tests for data collection forms and assisting in design of certification procedures.
  • Perform daily activities for clinical trials; respond to clinical site questions regarding data collection and data entry issues.
  • Coordinate scheduling a preparation of trial-related procedures and subject visits.
  • Work closely with clinical trial home infusion company to coordinate subject visits and documentation.
  • Develop brochures or other materials for providers to support recruitment of study participants.
  • Attend training sessions as needed for the implementation of clinical trials.

For a full job description, please email pedsuichildrens@healthcare.uiowa.edu.
About the Department of Pediatrics:
The Stead Family Department of Pediatrics is a national leader pediatric medicine. The Department's mission is to provide outstanding care to the children of Iowa and beyond by being a leader in state-of-the-art clinical care to children, 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 UI Stead Family Children's Hospital. UI Stead Family Children's Hospital is one of the nation's top-ranked pediatric care and research institutions, and Iowa's only comprehensive children's hospital.
PRV1 Required Qualifications:
  • Bachelor's degree in related field or an equivalency of education and/or related experience
  • Six months to one year of experience in clinical research.
  • Demonstrated excellent written, verbal, and interpersonal communication skills.
  • Knowledge of Institutional Review Board procedures, FDA regulations, GCP and study sponsor guidelines related to clinical trial research.
  • Demonstrated high attention to detail with strong organizational skills.

Highly Desirable Qualifications:
  • Six months to one year of experience in clinical trial protocol management.
  • Six months to one year of experience in data entry and management.
  • Demonstrated knowledge of or experience with medical genetic and lysosomal storage disorders.
  • Willingness and ability to travel.

PRV2 Required Qualifications:
  • Bachelor's degree in related field or an equivalency of education and/or related experience
  • Minimum of two years of experience in clinical trial protocol management, including but not limited to preparation of regulatory submissions, recruitment of eligible patients, and reporting of study data
  • Demonstrated excellent written, verbal, and interpersonal communication skills.
  • Knowledge of Institutional Review Board procedures, FDA regulations, GCP and study sponsor guidelines related to clinical trial research.
  • Demonstrated high attention to detail with strong organizational skills.
    Highly Desirable Qualifications:
  • One to three years of experience in clinical trial protocol management.
  • One to three years of experience in data entry and management.
  • Demonstrated knowledge of or experience with medical genetic and lysosomal storage disorders.
  • Willingness and ability to travel.
  • CRC (Certified Clinical Research Coordinator) or CCRP (Certified Clinical Research Professional) certification, or a Master's degree in a related field (e.g. MPH)

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

Pediatrics will be filling this position at one of two levels. The Clinical Trials Research Assistant position 3A salary range is $43,240-$66,199, and the Clinical Trials Research Associate position 4A salary range is $47,380-$79,386. You must indicate in your cover letter the level of classification (3A/4A) you wish to be considered for or indicate both. See required qualifications for additional information.
Job openings are posted for a minimum of 14 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 Bradley at Pedsuichildrenshr@healthcare.uiowa.edu.
This position is not eligible for university sponsorship for employment authorization.

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