ZipRecruiter

Log In

2

Remote Temporary Clinical Research Jobs in Kansas

Icon plc

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 ...

Icon plc

Clinical Research Associate II

Lenexa, KS · Remote

Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ... Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is ...

Icon plc

Clinical Research Associate II

Lawrence, KS · Remote

Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ... Willingness to travel as required (approximately 60%) #LI-LB1 #LI-REMOTE Employment with ICON is ...

Icon plc

CRA II

Lawrence, KS · Remote

$91K - $114K/yr

CRA II (Home-based in U.S.) ICON is a global healthcare intelligence and clinical research ... MM2 #LI-Remote Employment with ICON is contingent upon having the legal right to work in the ...

410 ICR United States USA

CRA II

Lawrence, KS · Remote

$91K - $114K/yr

CRA II (Home-based in U.S.) ICON is a global healthcare intelligence and clinical research ... MM2 #LI-Remote Employment with ICON is contingent upon having the legal right to work in the ...

Premier Research

Premier Research is looking for a Clinical Lead II, Oncology (Contract) to join our Clinical ... This is a 1 year remote-based contract position. What You'll Be Doing: * Serves as initial point of ...

next page

Showing results 1-20

All JobsClinical Research JobsRemote Temporary Clinical Research JobsRemote Temporary Clinical Research Jobs in Kansas

Remote Temporary Clinical Research information

What is the difference between Remote Temporary Clinical Research vs Remote Temporary Clinical Data Coordinator?

AspectRemote Temporary Clinical ResearchRemote Temporary Clinical Data Coordinator
CredentialsTypically requires a background in life sciences, clinical research certifications (e.g., CCRP), or related degreesRequires experience with data management, often with certifications like CDMP or related training
Work EnvironmentConducted remotely, often in research organizations or pharmaceutical companiesRemote data entry and management within clinical trial settings
Employer & Industry UsageUsed by biotech, pharma, and research institutions for trial oversightCommon in clinical research sites, CROs, and pharmaceutical companies for data handling

Remote Temporary Clinical Research involves overseeing or supporting clinical trials, requiring scientific knowledge and regulatory understanding. In contrast, Remote Temporary Clinical Data Coordinators focus on managing and entering trial data, emphasizing data accuracy and software skills. Both roles are remote, but they serve different functions within the clinical research process.

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

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

What are popular job titles related to Remote Temporary Clinical Research jobs in Kansas?

For Remote Temporary Clinical Research jobs in Kansas, the most frequently searched job titles are:

What job categories do people searching Remote Temporary Clinical Research jobs in Kansas look for?

The top searched job categories for Remote Temporary Clinical Research jobs in Kansas are:

What cities in Kansas are hiring for Remote Temporary Clinical Research jobs?

Cities in Kansas with the most Remote Temporary Clinical Research job openings:

Remote Temporary Clinical Research jobs near you
Infographic showing various Remote Temporary Clinical Research job openings in Kansas as of August 2026, with employment types broken down into 4% Internship, 71% Full Time, 6% Part Time, 13% Temporary, and 6% Contract. Highlights an 5% Hybrid, and 95% Remote job distribution.

Clinical Research Associate II / Senior Clinical Research Associate

Icon plc

On-site, Remote

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 5 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

Apply