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Clinical Data Associate Remote Jobs in Kansas (NOW HIRING)

ICON

Clinical Research Associate - St Louis/Kansas City/Ohio ICON plc is a world-leading healthcare ... Performing data review and resolution of queries to maintain high-quality clinical data.

Altasciences

Data Manager II

Overland Park, KS · On-site +1

Provide electronic data capture (EDC) system training (via WebEx) for clinical research associates (CRAs) and sponsor representatives. * Lead and/or participate in user acceptance testing (UAT) for ...

HaysMed

Remote HIM Coder II

Hays, KS · Remote

$17.25 - $23/hr

Associates Degree * Meditech Experience * 3M Computer Assisted Coding Experience Essential Duties ... Abstracts clinical data from health records and assigns appropriate ICD-10-CM/PCS and CPT codes, as ...

HaysMed

Remote HIM Coder II

Hays, KS · On-site +1

$19 - $27/hr

Associates Degree * Meditech Experience * 3M Computer Assisted Coding Experience Essential Duties ... Abstracts clinical data from health records and assigns appropriate ICD-10-CM/PCS and CPT codes, as ...

NTT DATA

Customer Service Associate

Wichita, KS · Remote

$15.50/hr

NTT DATA will provide a computer and headset for remote work. * Employees are responsible for the care and security of all equipment provided. They must return it immediately upon separation from the ...

NTT DATA Services

Customer Service Associate

Wichita, KS · Remote

$15.50/hr

NTT DATA will provide a computer and headset for remote work. * Employees are responsible for the care and security of all equipment provided. They must return it immediately upon separation from the ...

NTT DATA Services

Customer Service Associate

Wichita, KS · Remote

$15.50/hr

NTT DATA will provide a computer and headset for remote work. * Employees are responsible for the care and security of all equipment provided. They must return it immediately upon separation from the ...

NTT DATA Services

Customer Service Associate

Wichita, KS · Remote

$15.50/hr

We are currently seeking a Customer Service Associate to join our team. This position is eligible ... NTT DATA will provide a computer and headset for remote work. \t * Employees are responsible for ...

Ascend Learning

Data Import Specialist

Leawood, KS · On-site +1

Headquartered in Burlington, MA, with additional office locations and hybrid and remote workers in ... clinical practice. We use data analytics and engaging learning tools to help nursing students ...

Remote - Referral Board

Maintain accurate CRM data and pipeline tracking * Assist in managing high-velocity opportunities and timely follow-up * Develop a strong understanding of Remote's PEO offering and market positioning

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Clinical Data Associate Remote information

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$11

$36

$77

How much do clinical data associate remote jobs pay per hour?

As of Jun 12, 2026, the average hourly pay for clinical data associate remote in Kansas is $36.13, according to ZipRecruiter salary data. Most workers in this role earn between $25.29 and $45.29 per hour, depending on experience, location, and employer.

What are some common challenges faced by a Clinical Data Associate working remotely, and how can they be managed?

Clinical Data Associates working remotely often face challenges related to communication and maintaining data quality standards across distributed teams. It can be more difficult to collaborate with clinical research coordinators, data managers, and other stakeholders without in-person interactions, making clear and timely communication essential. Utilizing secure data management platforms, participating in regular virtual meetings, and adhering strictly to data integrity protocols can help address these challenges. Proactively seeking feedback and staying updated on regulatory changes also contribute to maintaining high standards while working remotely.

What is a Clinical Data Associate (Remote)?

A Clinical Data Associate (Remote) is a professional who manages and verifies data collected during clinical trials, working from a remote location. They ensure the accuracy, integrity, and confidentiality of clinical trial data, collaborating with clinical teams and using specialized software. Their responsibilities include data entry, cleaning, validation, and generating reports to support regulatory submissions. Remote Clinical Data Associates utilize secure systems to access and manage data, allowing them to efficiently support clinical research from anywhere.

What are the key skills and qualifications needed to thrive as a Clinical Data Associate (Remote), and why are they important?

To thrive as a Clinical Data Associate (Remote), you need a strong background in life sciences, data management, and an understanding of clinical trial processes, often supported by a relevant bachelor's degree. Familiarity with electronic data capture (EDC) systems, clinical data management software, and GCP (Good Clinical Practice) certification are commonly required. Attention to detail, problem-solving abilities, and effective virtual communication are crucial soft skills for managing data integrity and collaborating with remote teams. These skills and qualifications ensure the accurate collection, validation, and reporting of clinical trial data, which is essential for regulatory compliance and successful study outcomes.

What is the difference between Clinical Data Associate Remote vs Clinical Data Coordinator?

AspectClinical Data Associate RemoteClinical Data Coordinator
CredentialsBachelor's in life sciences or related field; familiarity with data management systemsBachelor's in health sciences or related field; experience with clinical data
Work EnvironmentRemote, primarily computer-basedTypically on-site or hybrid, working with clinical teams
Employer & IndustryPharmaceutical companies, CROs, biotech firmsHospitals, research institutions, clinical trial sites
Search & Comparison IntentYesYes

The Clinical Data Associate Remote and Clinical Data Coordinator roles share similarities in required education and industry usage. However, Clinical Data Associate Remote positions are primarily remote and focus on data entry and management from a distance, while Clinical Data Coordinators often work on-site, coordinating data collection and quality at clinical sites. Both roles are essential in clinical research but differ mainly in work setting and specific responsibilities.

What are popular job titles related to Clinical Data Associate Remote jobs in Kansas? For Clinical Data Associate Remote jobs in Kansas, the most frequently searched job titles are:
What job categories do people searching Clinical Data Associate Remote jobs in Kansas look for? The top searched job categories for Clinical Data Associate Remote jobs in Kansas are:
What cities in Kansas are hiring for Clinical Data Associate Remote jobs? Cities in Kansas with the most Clinical Data Associate Remote job openings:
Clinical Data Associate Remote jobs near you
Clinical Research Associate

Clinical Research Associate

ICON

On-site, Remote

Full-time

Medical, Life, Retirement, PTO

Posted 25 days ago

Job description

Clinical Research Associate - St Louis/Kansas City/Ohio
ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development
We are currently seeking a Clinical Research Associate to join our diverse and dynamic team. As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.
What you will be doing
  • Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
  • Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
  • Collaborating with investigators and site staff to facilitate smooth study conduct.
  • Performing data review and resolution of queries to maintain high-quality clinical data.
  • Contributing to the preparation and review of study documentation, including protocols and clinical study reports

Your profile
  • Bachelor's degree in a scientific or healthcare-related field.
  • Minimum of 9 months onsite monitoring experience as a Clinical Research Associate; level (CRA I, CRA II, or Senior CRA) determined by total years of experience. In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
  • Strong organizational and communication skills, with attention to detail.
  • Ability to work independently and collaboratively in a fast-paced environment.
  • Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver's license.

What ICON can offer you:
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family's needs.
  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
  • Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family's well-being.
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here.
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here to apply

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