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Clinical Research Training Jobs in Iowa (NOW HIRING)

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Clinical Research Training information

See Iowa salary details

$12

$22

$38

How much do clinical research training jobs pay per hour?

As of May 28, 2026, the average hourly pay for clinical research training in Iowa is $22.63, according to ZipRecruiter salary data. Most workers in this role earn between $18.94 and $23.27 per hour, depending on experience, location, and employer.

What is a Clinical Research Training job?

A Clinical Research Training job involves developing, organizing, and delivering educational programs for clinical research professionals. This role ensures that researchers, coordinators, and other staff understand regulatory requirements, ethical considerations, and best practices in clinical trials. Responsibilities may include creating training materials, conducting workshops, and maintaining compliance with industry standards. It is essential for ensuring the integrity and effectiveness of clinical research studies.

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

To excel in Clinical Research Training, you typically need a background in life sciences or healthcare, familiarity with clinical trials, and strong organizational abilities. Experience with learning management systems (LMS), Good Clinical Practice (GCP) certification, and proficiency in relevant regulatory documentation tools is highly beneficial. Outstanding soft skills include excellent communication, instructional ability, attention to detail, and adaptability to evolving protocols. These competencies are crucial for effectively educating clinical staff, ensuring compliance, and maintaining high-quality research standards.

What does a typical day look like for someone working in Clinical Research Training?

A typical day in Clinical Research Training often involves developing and delivering training materials for research staff, conducting onboarding sessions for new team members, and ensuring all participants meet regulatory and protocol requirements. Trainers may collaborate closely with investigators, study coordinators, and regulatory teams to assess learning needs and update curricula as guidelines evolve. The role also includes monitoring training records, organizing workshops or seminars, and providing support for staff questions on GCP and compliance. This dynamic work environment offers opportunities for continuous professional development and direct impact on the success and integrity of clinical research projects.
What are popular job titles related to Clinical Research Training jobs in Iowa? For Clinical Research Training jobs in Iowa, the most frequently searched job titles are:
Infographic showing various Clinical Research Training job openings in Iowa as of May 2026, with employment types broken down into 1% As Needed, 89% Full Time, 8% Part Time, and 2% Contract. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $47,064 per year, or $22.6 per hour.
Clinical Research Assistant (CRA) - Innovo Research in partnership with The Iowa Clinic

Clinical Research Assistant (CRA) - Innovo Research in partnership with The Iowa Clinic

The Iowa Clinic

West Des Moines, IA • On-site

Full-time

This job post has expired today. Applications are no longer accepted.


The Iowa Clinic rating

7.0

Company rating: 7.0 out of 10

Based on 16 frontline employees who took The Breakroom Quiz


Job description

A day in the life…
Wondering what a day in the life of a Clinical Research Assistant at Innovo Research might look like?
  • Coordinate key study activities—from start-up to close-out—by staying organized, responsive, and protocol-focused. 
  • Support providers and study representatives as a liaison, helping keep communication clear across the research team and patients. 
  • Recruit, screen, and schedule prospective participants using medical records, databases, referrals, and community outreach. 
  • Help guide the informed consent process (as delegated and required) and document interactions according to protocol and regulatory standards. 
  • Support study visits by collecting medical information, performing or arranging phlebotomy, and preparing/handling labs for shipment and review. 
  • Maintain accurate study documentation (source, case report forms, and regulatory files) and keep supplies stocked for protocol needs. 
  • Prepare for monitor visits and support ongoing regulatory compliance while protecting patient privacy and confidentiality. 
 
This job might be for you if you have…
Qualifications
  • High school diploma or equivalent (Bachelor’s degree preferred). 
  • Experience in a clinical setting (2–5 years a plus), with comfort working directly with patients. 
  • Strong organization, attention to detail, and ability to maintain accurate records and documentation. 
  • Clear written and verbal communication skills and the ability to work effectively with providers, sponsors/monitors, and internal teams. 
  • Comfort using computers, email, and standard office/clinical systems (EMR and scheduling experience a plus). 
  • Commitment to confidentiality and ethical conduct in a clinical research environment (GCP and FDA/OSHA knowledge a plus). 
 
Bonus points if…
  • You have phlebotomy experience or certification and are comfortable with sample handling/shipping. 
  • You have CNA/medical assistant training or similar hands-on clinical education. 
  • You enjoy a fast-paced clinic environment, stay calm when priorities change, and take pride in quality documentation. 
 
This role is in-person at a site-specific clinic location; standard schedule is 40 hours/week, with occasional evenings/weekends as needed.

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