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Entry Level Clinical Research Associate Jobs in Kansas

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About the Opportunity As a Clinical Research Associate within our sponsor-dedicated environment, you will play a critical role in the successful delivery of clinical trials, helping bring innovative ...

IQVIA

Clinical Research Associate

Overland Park, KS · On-site

$71K - $189K/yr

Clinical Research Associate II & Senior Clinical Research Associate (CRA II/Sr. CRA) Multiple Therapeutic Areas | Nationwide Opportunities IQVIA is actively seeking experienced Clinical Research ...

ICON

Senior Medical Research Associate

Lenexa, KS · On-site

Senior Medical Research Associate (Paramedic) - Lenexa, KS (Onsite) ICON is a global healthcare ... We advance clinical research by providing outsourced services to pharmaceutical, biotechnology ...

Alira Health

Clinical Research Associate

Bern, KS · On-site

Summary ROLE The Clinical Research Associate is an important member of the Alira Health Clinical team. CRAs are highly motivated and function independently to conduct site monitoring responsibilities ...

IQVIA

Clinical Research Associate

Overland Park, KS · On-site

$71K - $189K/yr

Basic knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines)

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Entry Level Clinical Research Associate information

What is an entry level clinical research associate?

An Entry Level Clinical Research Associate (CRA) is responsible for monitoring clinical trials to ensure compliance with regulatory requirements, ethical guidelines, and study protocols. They assist in site selection, data collection, and verifying that study procedures are properly followed. Entry-level CRAs typically work under the supervision of senior CRAs and may travel to different clinical sites. Strong attention to detail, knowledge of Good Clinical Practice (GCP) guidelines, and organizational skills are essential. This role is a starting point for a career in clinical research, with opportunities for growth into senior CRA or project management positions.

What are the typical daily responsibilities of an entry level clinical research associate?

As an Entry Level Clinical Research Associate, your day-to-day work generally involves assisting with monitoring clinical trial sites, reviewing study documentation, and ensuring adherence to protocol and regulatory requirements. You may support more senior team members in conducting on-site or remote visits, tracking patient recruitment, and managing data collection. Additionally, you’ll communicate regularly with site staff and other stakeholders to resolve issues and ensure data quality. This hands-on experience is essential for building expertise in clinical research processes and advancing toward more senior CRA roles.

What are the key skills and qualifications needed to thrive as an entry level clinical research associate?

To thrive as an Entry Level Clinical Research Associate, you typically need a bachelor's degree in life sciences or a related field, a solid understanding of clinical trial protocols, and attention to detail. Familiarity with Good Clinical Practice (GCP) guidelines, electronic data capture (EDC) systems, and regulatory documentation is often required. Strong communication, organization, and problem-solving abilities help you effectively collaborate with study sites and team members. These skills are critical to ensure the accuracy, compliance, and successful progression of clinical studies.

What are the most commonly searched types of Entry Level Clinical Research jobs in Kansas?

The most popular types of Entry Level Clinical Research jobs in Kansas are:

What are popular job titles related to Entry Level Clinical Research Associate jobs in Kansas?

For Entry Level Clinical Research Associate jobs in Kansas, the most frequently searched job titles are:

What job categories do people searching Entry Level Clinical Research Associate jobs in Kansas look for?

The top searched job categories for Entry Level Clinical Research Associate jobs in Kansas are:

What cities in Kansas are hiring for Entry Level Clinical Research Associate jobs?

Cities in Kansas with the most Entry Level Clinical Research Associate job openings:

Entry Level Clinical Research Associate jobs near you
Infographic showing various Entry Level Clinical Research 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.

Clinical Research Associate II / Senior Clinical Research Associate

On-site, Remote

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Full-time

Medical, Dental, Vision, Life, Retirement

Posted 17 days ago

Job description

North America | Remote | Sponsor-Dedicated (FSP) Opportunities

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.


At ICON Strategic Solutions, we're continually growing our network of talented Clinical Research Associates across North America. As we expand our partnerships with leading global sponsors, we are seeking experienced CRA II and Senior CRA professionals interested in sponsor-dedicated opportunities.

About the Opportunity

As a Clinical Research Associate within our sponsor-dedicated environment, you will play a critical role in the successful delivery of clinical trials, helping bring innovative therapies to patients worldwide.

Depending on your experience level, you may:

  • Conduct site qualification, initiation, routine monitoring, and close-out visits
  • Ensure protocol compliance, patient safety, data quality, and regulatory adherence
  • Build strong relationships with investigative sites and key stakeholders
  • Identify and proactively resolve site and study issues
  • Collaborate with cross-functional teams to support successful study delivery
  • Support inspection readiness and high-quality study execution
  • Mentor and guide less experienced CRAs (Senior CRA level)

What We're Looking For

CRA II

  • Bachelor's degree in a scientific, healthcare, or related field
  • Clinical monitoring experience within the pharmaceutical, biotech, or CRO industry
  • Strong knowledge of ICH-GCP, clinical trial regulations, and monitoring practices
  • Ability to work independently while collaborating effectively across teams

Senior CRA

  • Significant clinical monitoring experience across multiple studies and sites
  • Advanced knowledge of clinical trial processes, regulations, and site management
  • Proven ability to manage priorities and drive study quality independently
  • Experience mentoring or supporting other CRAs is advantageous

For all applicants

  • Strong communication and relationship-building skills
  • Willingness to travel as required
  • Passion for advancing clinical research and improving patient outcomes

When you join ICON Strategic Solutions, you gain the best of both worlds:

  • Work within dedicated sponsor environments
  • Build expertise with leading global pharmaceutical and biotechnology companies
  • Access diverse opportunities across multiple therapeutic areas
  • Benefit from ICON's global scale, career development, and support network
  • Join a culture focused on innovation, collaboration, and patient impact
  • Competitive compensation and benefits package

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 requesthere.

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

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