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Senior Clinical Research Associate Jobs in Iowa (NOW HIRING)

CVAUSA

Clinical Research Coordinator

Davenport, IA · On-site

$60 - $80/hr

Clinical Research Coordinator Location: On-site position in Davenport, Iowa About CVAUSA ... Cardiovascular Associates of America (CVAUSA) is a rapidly growing leader in cardiovascular care ...

Pella Regional Health Center

Clinical Research

Pella, IA · On-site

$9/hr

RN - Clinical Research Travel position with normal urgency. Regular pay rate is $9. Shift details include an 8-hour day shift, 5 shifts per week, and 40 scheduled hours. The job order starts on 07/07 ...

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Iterative Health

Clinical Research Coordinator II

Waterloo, IA · On-site

$24 - $31.75/hr

Associate's or Bachelor's degree in a scientific, healthcare, or related discipline required * 3-5 years of clinical research or healthcare experience required * CCRC ® - Certified Clinical Research ...

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Senior Clinical Research Associate information

See Iowa salary details

$33.8K

$88.6K

$134.8K

How much do senior clinical research associate jobs pay per year?

As of Sep 7, 2026, the average yearly pay for senior clinical research associate in Iowa is $88,586.00, according to ZipRecruiter salary data. Most workers in this role earn between $58,700.00 and $120,200.00 per year, depending on experience, location, and employer.

What does a senior clinical research associate do?

A senior clinical research associate (CRA) monitors clinical trials and manages team members. Your duties include leading project team meetings, running experiments, making observations, tracking results, and analyzing data. You also ensure experiments meet all clinical practice and safety standards. Qualifications for this career are a bachelor of science in a biomedical field or a bachelor of science in nursing (BSN), along with professional experience in a medical or research setting. You must have strong communication, interpersonal, leadership, and technical writing skills.

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

To thrive as a Senior Clinical Research Associate, you need a solid background in clinical research, regulatory compliance, and often a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and relevant certifications such as ACRP or SOCRA are typically required. Strong organizational skills, attention to detail, and the ability to communicate effectively with diverse stakeholders make someone stand out in this position. These skills and qualities are vital for ensuring studies are conducted ethically, accurately, and in compliance with regulatory standards.

What are some typical challenges faced by senior clinical research associates when overseeing multiple clinical trials?

Senior Clinical Research Associates (SCRAs) often manage several studies at once, which requires balancing competing deadlines, ensuring protocol compliance, and maintaining strong communication with site staff. A common challenge is ensuring consistent data quality and regulatory adherence across diverse sites, especially when trials are geographically dispersed. Effective time management, attention to detail, and proactive problem-solving are crucial for success in this role. Collaboration with project managers, investigators, and regulatory teams is also essential to ensure trials progress smoothly and meet all regulatory requirements.
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Senior Clinical Research Associate jobs near you
Infographic showing various Senior Clinical Research 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 $88,586 per year, or $42.6 per hour.

Clinical Research Coordinator

Cardiovascular-Associates-of-America

Davenport, IA • On-site

$60 - $80/hr

Other

Posted 10 days ago

Job description

Job Title: Clinical Research Coordinator
Location: On-site position in Davenport, Iowa

About CVAUSA:

Cardiovascular Associates of America (CVAUSA) is a rapidly growing leader in cardiovascular care, committed to advancing medical research and improving patient outcomes. As part of our expansion, we are increasing our clinical trial operations and looking for dynamic, results-driven professionals to join our team.

At CVAUSA, we are focused on innovation and excellence in cardiovascular research, and we believe the best results come from individuals who are passionate about making a difference.

The Research Coordinator will be responsible for leading the growth and development of the research program while also working with clinic staff on existing and new clinical trials. As part of CVAUSA’s national network, the Clinical Research Coordinator will have the opportunity to collaborate with teams across the country, making an impact on cardiovascular care both locally and nationwide.

Position Overview:

As a Clinical Research Coordinator, you will play a key role in managing and overseeing all aspects of clinical trials and site operations. You will have the opportunity to take ownership of your projects, driving them forward with innovation, efficiency, and excellence. This is a fantastic opportunity for an ambitious, goal-oriented individual who thrives in an independent, fast-paced environment.

Key Responsibilities:

Clinical Trial Management:
Oversee all aspects of clinical trials, including patient recruitment, screening, and enrollment. Ensure that protocols are followed meticulously.

Site Operations:
Handle day-to-day site management, ensuring that all activities comply with regulatory requirements and study protocols.

Data Management:
Collect, verify, and manage clinical trial data, ensuring it is accurate and complete.

Communication & Reporting:
Act as the primary point of contact for study sponsors, participants, and other stakeholders. Provide regular updates and progress reports.

Regulatory Compliance:
Ensure all documentation, including regulatory submissions and patient records, are kept up-to-date and in compliance with ethical and legal standards.

Problem Solving & Innovation:
Identify areas for process improvement and implement solutions to drive efficiency and enhance trial operations.

What We’re Looking For:

Goal-Driven & Independent:
You thrive in an autonomous work environment and take full ownership of your responsibilities.

Innovative & Results-Driven:
You are eager to contribute to CVAUSA’s growth and bring effective solutions to the table.

Detail-Oriented & Highly Organized:
You have the ability to manage multiple tasks and deadlines without sacrificing quality.

Strong Communicator:
You can effectively communicate with stakeholders at all levels, including sponsors, site staff, and participants.

Experience & Qualifications:
  • Clinical experience in cardiovascular medicine in a licensed or clinical support role (e.g., RN, technologist, medical assistant)
  • Bachelor’s degree in a relevant field (e.g., life sciences, healthcare, or clinical research)
  • Experience managing clinical trials, leading enrollment across multiple studies, and supporting research program development
  • Strong organizational and time management skills
  • Clinical research certification (e.g., CCRP) is a plus
  • Knowledge of GCP, ICH guidelines, and regulatory requirements
Why CVAUSA?

At CVAUSA, we believe in the power of innovation and are looking for professionals eager to make an impact in cardiovascular research. As a rapidly growing organization, you will be at the forefront of cutting-edge clinical trials, contributing to improved patient outcomes.

You will work on-site in Davenport, Iowa, leading a growing cardiovascular research program while collaborating with teams nationwide. We offer competitive compensation, flexible working hours, and a supportive, dynamic environment where your contributions are valued.

If you are ambitious, innovative, and ready to take your career to the next level, we want to hear from you.

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