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Clinical Study Associate Jobs in Kansas (NOW HIRING)

People People

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 ...

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 ...

VCA Animal Hospitals

Associate Veterinarian

Andover, KS · On-site

Join us as an Associate Veterinarian, DVM at VCA Andover Animal Hospital and Pet Resort located in ... Opportunities to participate in a robust Clinical Studies program Discover Additional Benefits ...

VCA Animal Hospitals

Associate Veterinarian

Andover, KS · On-site

Join us as an Associate Veterinarian, DVM at VCA Andover Animal Hospital and Pet Resort located in ... Opportunities to participate in a robust Clinical Studies program Discover Additional Benefits ...

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Clinical Study Associate information

See Kansas salary details

$11

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$49

How much do clinical study associate jobs pay per hour?

As of Sep 10, 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 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 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 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 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 August 2026, with employment types broken down into 2% As Needed, 75% Full Time, 16% Part Time, 1% Temporary, and 6% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $58,509 per year, or $28.1 per hour.

Clinical Pathology Technician

Bucyrus, KS • On-site

People People
Construction • 1 - 10 employees
Learn more about People Peopleexternal

$18 - $23/hr

Other

Medical, Dental, Vision, Retirement

Re-posted 8 days ago

Job description

Pathology Technician

How would you like to have a career that really makes a difference? Attentive Science is a nimble Non-Clinical Contract Research Organization (CRO) providing support to the Pharmaceutical, Animal Health, Agrochemical and Food Industries to help them create a healthier future for us all. Our experienced scientists provide the highest quality results coupled with segment leading expediency and flexible solutions to meet the specific needs of our clients.

The Pathology Technician is responsible for test article coordination for maintaining the company chemical and reaction inventory in accordance with the Good Laboratory Practice (GLP) and company requirements.

What will you be doing?

  • Perform clinical pathology assays including hematology, coagulation, urinalysis, and clinical chemistry on animal samples (e.g., rodents, non-rodents).
  • Prepare, handle, and process biological samples (blood, urine, plasma, serum, etc.) according to study protocols and SOPs.
  • Operate, calibrate, and maintain analytical instruments such as hematology analyzers, chemistry analyzers, and urinalysis systems.
  • Review and record test results accurately, ensuring data integrity and compliance with GLP documentation requirements.
  • Manage proper sample tracking and inventory records.
  • Assist with data entry, quality control checks, and generation of study reports.
  • Support validation and troubleshooting of instruments and methodologies as needed.
  • Maintain laboratory supplies, ensure proper labeling and storage of samples, and adhere to biosafety and other protocols.
  • Collaborate with other laboratory teams (e.g., toxicology, necropsy, bioanalytical) to ensure efficient sample management and workflow.
  • Participate in internal and external audits as required.
  • Other duties as assigned.

Education & Preferred Experience:

  • Associate's or Bachelor's degree in Medical Laboratory Science, Biology, Animal Science, or a related scientific field preferred.
  • 1–3 years of experience in a clinical pathology or clinical laboratory setting preferred.
  • Experience in a non-clinical GLP-regulated CRO environment highly desirable.
  • Familiarity with preclinical research procedures preferred.
  • Working knowledge of laboratory instrumentation, analytical methods, and quality control practices.
  • Strong attention to detail and data accuracy.
  • Ability to work independently and collaboratively in a fast-paced, deadline-driven environment.
  • Proficient computer skills (LIMS, Microsoft Office Suite).
  • Excellent communication and organizational skills.

Join the Attentive Science team and grow your career with us while contributing to the discovery and development of life saving remedies. Attentive Science provides a comprehensive benefits package including Healthcare, Dental, Vision, 401k and on-the-job career development.

Apply