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Clinical Study Associate Jobs in Kansas (NOW HIRING)

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Clinical Pathology Technician

Bucyrus, KS · On-site

$18 - $23/hr

... study protocols and SOPs. * Operate, calibrate, and maintain analytical instruments such as ... Associate's or Bachelor's degree in Medical Laboratory Science, Biology, Animal Science, or a ...

People People

Clinical Pathology Technician

Stilwell, KS · On-site

$18.75 - $24.25/hr

... study protocols and SOPs. * Operate, calibrate, and maintain analytical instruments such as ... Associate's or Bachelor's degree in Medical Laboratory Science, Biology, Animal Science, or a ...

People People

Clinical Pathology Technician

Stilwell, KS · On-site

$18.75 - $24.25/hr

... study protocols and SOPs. * Operate, calibrate, and maintain analytical instruments such as ... Associate's or Bachelor's degree in Medical Laboratory Science, Biology, Animal Science, or a ...

People People

Clinical Pathology Technician

Stilwell, KS · On-site

$18.75 - $24.25/hr

... study protocols and SOPs. * Operate, calibrate, and maintain analytical instruments such as ... Associate's or Bachelor's degree in Medical Laboratory Science, Biology, Animal Science, or a ...

People People

Clinical Pathology Technician

Stilwell, KS

$18.75 - $24.25/hr

... study protocols and SOPs. * Operate, calibrate, and maintain analytical instruments such as ... Associate's or Bachelor's degree in Medical Laboratory Science, Biology, Animal Science, or a ...

IQVIA

Clinical Research Associate

Overland Park, KS

$71K - $189K/yr

... Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Work with ... Administer protocol and related study training to assigned sites and establish regular lines of ...

IQVIA

Clinical Research Associate

Overland Park, KS

$71K - $189K/yr

... Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Work with ... Administer protocol and related study training to assigned sites and establish regular lines of ...

IQVIA

Clinical Research Associate

Overland Park, KS

$87K - $182K/yr

... Clinical Practice. Work with sites to adapt, drive, and track subject recruitment plan in line with ... Administer protocol and related study training to assigned sites and establish regular lines of ...

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All JobsClinical Study Associate JobsClinical Study Associate Jobs in Kansas

Clinical Study Associate information

See Kansas salary details

$11

$28

$49

How much do clinical study associate jobs pay per hour?

As of Aug 5, 2026, the average hourly pay for clinical study associate in Kansas is $28.13, according to ZipRecruiter salary data. Most workers in this role earn between $18.85 and $37.07 per hour, depending on experience, location, and employer.

What is a clinical study associate?

Clinical Study Associates (CSAs) are professionals who support the planning, execution, and monitoring of clinical trials in the pharmaceutical, biotechnology, or medical device industries. They help coordinate study logistics, maintain study documentation, and ensure compliance with regulatory requirements. CSAs often work closely with Clinical Research Associates, study coordinators, and investigators to ensure that trials are conducted according to protocol and timelines. Their role is essential in ensuring the accuracy and integrity of data collected during clinical research.

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

AspectClinical Study AssociateClinical Research Coordinator
CredentialsBachelor's degree, often in life sciences; certifications like CCRP or CCRA beneficialBachelor's degree in health sciences or related field; certifications like CCRP advantageous
Work EnvironmentPharmaceutical companies, CROs, clinical trial sitesHospitals, clinics, research centers
Job FocusMonitoring clinical trials, ensuring protocol compliance, data accuracyManaging daily trial activities, patient recruitment, data collection
Employer & Industry UsageCommonly employed in pharma and CROsPrimarily in healthcare and academic research settings

Both roles involve clinical trial oversight but differ in focus: Clinical Study Associates primarily monitor and ensure compliance during trials, while Clinical Research Coordinators manage daily trial operations and patient interactions. Understanding these distinctions helps in choosing the right career path or job search focus.

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

To thrive as a Clinical Study Associate, you need a strong understanding of clinical research processes, regulatory requirements, and typically a life sciences degree. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and GCP certification are commonly required. Attention to detail, organizational skills, and effective communication set top performers apart in this role. These competencies ensure accurate study documentation, regulatory compliance, and smooth coordination across research teams.

What are some common challenges clinical study associates face when managing multiple clinical trials simultaneously?

Clinical Study Associates often juggle several clinical trials at once, which can present challenges such as prioritizing competing deadlines, maintaining accurate documentation for each study, and ensuring consistent communication with cross-functional teams. Staying organized and proactive is essential, as unforeseen protocol amendments or site issues can arise. Building strong relationships with site staff and utilizing effective project management tools can help CSAs navigate these complexities and deliver high-quality results.
What are the most commonly searched types of Clinical Study jobs in Kansas? The most popular types of Clinical Study jobs in Kansas are:
What cities in Kansas are hiring for Clinical Study Associate jobs? Cities in Kansas with the most Clinical Study Associate job openings:
Clinical Study Associate jobs near you
Infographic showing various Clinical Study Associate job openings in Kansas as of July 2026, with employment types broken down into 1% As Needed, 71% Full Time, 25% Part Time, 1% Temporary, and 2% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $58,509 per year, or $28.1 per hour.

Senior Clinical Research Associate

410 ICR United States USA

Lenexa, KS • Remote

Full-time

Posted 14 days ago

Job description

Senior CRA / CRA II - United States - Home Based

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.


As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.

What You Will Do:

You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement.
Key responsibilities include:

  • Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
  • Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
  • Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.
  • Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
  • Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Your Profile:

You will have a strong foundation in clinical trial monitoring, with the experience to work independently and guide others.
Required qualifications and experience:

  • Bachelor's degree in a relevant scientific discipline or healthcare-related field
  • 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 simultaneously, with strong organizational and problem-solving skills.
  • Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
  • Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.
  • Willingness to travel as required (approximately 60%)
     

    #LI-LB1 #LI-REMOTE


Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


Visit our careers site to read more about the benefits ICON offers.


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Are you a current ICON Employee? Please click here to apply