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Medical Research Assistant Jobs in Kansas (NOW HIRING)

Johnson County Clin Trials

Research Assistant

Lenexa, KS · On-site

$25/hr

Certification as a Medical Assistant is preferred. * At least one year of experience in medical history, medication history, and vital signs preferred. * Familiarity with clinical trial management ...

Johnson County Clintrials

Research Assistant

Lenexa, KS · On-site

$25/hr

Certification as a Medical Assistant is preferred. * At least one year of experience in medical history, medication history, and vital signs preferred. * Familiarity with clinical trial management ...

New

ICON

Senior Medical Research Associate

Lenexa, KS · On-site

Senior Medical Research Associate (Paramedic) - Lenexa, KS (Onsite) ICON is a global healthcare ... Research & Operational Responsibilities * Assist in planning, coordinating, and executing clinical ...

The Land Institute

Seasonal Research Assistants

Salina, KS · On-site

$14 - $18/hr

Research Assistant - Temporary This position requires in-person work in Salina, KS. This position is not eligible for any type of sponsorship for work authorization at this time. Who We Are + What We ...

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How much do medical research assistant jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for medical research assistant in Kansas is $17.74, according to ZipRecruiter salary data. Most workers in this role earn between $15.24 and $19.52 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a medical research assistant?

A Medical Research Assistant should have a background in life sciences or a related field, strong analytical skills, and experience with laboratory techniques. Familiarity with lab equipment, data analysis software (such as SPSS or Excel), and knowledge of research protocols or compliance standards like IRB procedures are commonly required. Attention to detail, effective communication, and organizational skills are vital soft skills for managing data and collaborating within research teams. These competencies ensure accurate data collection, ethical research practices, and contribute to the overall success and reliability of scientific studies.

What are some typical challenges faced by medical research assistants when managing multiple research projects simultaneously?

Medical Research Assistants often juggle several research projects at once, which can present challenges such as balancing competing deadlines, ensuring data accuracy, and adhering to varying protocols. Effective organization and time management are crucial to keep studies on track and maintain compliance with regulatory standards. Collaboration with principal investigators, lab technicians, and other team members helps distribute tasks and streamline communication, but adapting to shifting priorities and maintaining attention to detail remain essential skills for success.

What is the difference between Medical Research Assistant vs Clinical Research Coordinator?

AspectMedical Research AssistantClinical Research Coordinator
CredentialsTypically requires a bachelor's degree in health sciences or related field; certifications like CCRA are optionalRequires a bachelor's degree; certifications like CCRP or CCRC are common
Work EnvironmentAssists in laboratory or clinical settings, supporting research activitiesManages clinical trials, interacts with patients, and oversees study protocols
Employer & IndustryHospitals, research institutes, universitiesPharmaceutical companies, hospitals, research organizations

Medical Research Assistants support research activities by assisting with data collection, lab work, and patient interactions. Clinical Research Coordinators oversee entire clinical trials, ensuring compliance and managing study logistics. Both roles require similar educational backgrounds but differ in responsibilities and scope within the research process.

How do I become a medical research assistant?

To become a medical research assistant, candidates typically need a bachelor's degree in a health-related field such as biology, nursing, or public health. Relevant skills include data collection, laboratory techniques, and familiarity with research protocols; some positions may require certification or training in specific tools or procedures. Gaining experience through internships or entry-level roles can also improve job prospects.

What does a medical research assistant do?

A medical research assistant supports clinical and laboratory research by collecting and analyzing data, managing study documentation, and assisting with experiments. They often work under the supervision of researchers or physicians and may use tools like electronic health records and data analysis software. Strong organizational skills and knowledge of medical terminology are important for this role.

What qualifications do I need to be a medical research assistant?

A medical research assistant typically needs a bachelor's degree in a health-related field such as biology, nursing, or public health. Relevant skills include attention to detail, data management, and familiarity with research protocols and tools like electronic health records or statistical software. Some positions may require certification or training in Good Clinical Practice (GCP) or human subjects research ethics.

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

The most popular types of Medical Research jobs in Kansas are:

What are popular job titles related to Medical Research Assistant jobs in Kansas?

For Medical Research Assistant jobs in Kansas, the most frequently searched job titles are:

What job categories do people searching Medical Research Assistant jobs in Kansas look for?

The top searched job categories for Medical Research Assistant jobs in Kansas are:

What cities in Kansas are hiring for Medical Research Assistant jobs?

Cities in Kansas with the most Medical Research Assistant job openings:

Medical Research Assistant jobs near you
Infographic showing various Medical Research Assistant job openings in Kansas as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 15% Part Time, 1% Temporary, and 6% Contract. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $36,896 per year, or $17.7 per hour.

Research Assistant

Johnson County Clin Trials

Lenexa, KS • On-site

$25/hr

Full-time

Posted 4 days ago

Job description

Job Type
Full-time
Description
Position: Research Assistant
Department: Clinical Operations
Purpose:
The Research Assistant supports clinical research operations by assisting Study Coordinators and the study team in executing clinical trial activities. This role ensures compliance with study protocols, Good Clinical Practice (GCP), and Standard Operating Procedures (SOPs) while maintaining confidentiality and high-quality standards.
Position Summary:
The Research Assistant provides administrative and operational support for clinical trials, including document preparation, data entry, subject recruitment, and protocol-specific activities such as vital signs and specimen collection. The position reports to the Site Manager or Site Director and works under the direction of Clinical Research Coordinators.
Key Responsibilities (Essential Functions):
  • Ensure the confidentiality of clinical research volunteers and sponsors
  • Maintain and advocate a high level of customer service and quality within the department
  • Assist in the maintenance of Clinical Conductor
  • Maintain the ERP system including preparing, filing, assisting with updates and archiving study related information
  • Perform data entry and query resolution
  • Prepare, handle, distribute, track and maintain clinical trial related supplies
  • Assist with the pre-screening, screening, recruiting and enrollment of research subjects as authorized
  • Assist with educating study volunteers on study procedures such as diary completion, electronic devices and expected outcomes in a profession and accountable manner following protocol requirements.
  • Assist in tracking volunteer visits in Clinical Conductor, rescheduling as needed and update study coordinators in a timely fashion regarding missed visits or compliance issues.
  • Perform protocol specific activities including but not limited to medical history, vital signs, electrocardiograms and specimen collection.
  • Record adverse events and concomitant medication use and follow-up on open adverse events until through resolution.
  • Obtain and document study related events and data in compliance with GCP/SOPs
  • Communicate necessary volunteer information in a timely manner to study coordinator/PI on an ongoing basis.
  • Assure source documents/charts are prepared for future study visits.
  • Proactively escalate issues and/or problems
  • Develop strong working relationships and maintain effective communication with study team members, Investigators and practice staff
  • May collect, process and ship laboratory specimens at certain sites and or as needed
  • Other duties as assigned

Education and Experience:
  • Required: High school diploma or GED.
  • Preferred: Bachelor's degree.
  • Experience in clinical research setting or related environment preferred.
  • Certification as a Medical Assistant is preferred.
  • At least one year of experience in medical history, medication history, and vital signs preferred.
  • Familiarity with clinical trial management systems is a plus.

Skills and Competencies:
  • Excellent communication (verbal and written) and interpersonal skills.
  • Bilingual: Proficiency in Spanish and English, including the ability to speak, read, and write in both languages is preferred.
  • Strong organizational and time management abilities.
  • Detail-oriented with high accuracy.
  • Proficiency in Microsoft Office Suite (Word, Excel, Outlook, PowerPoint, SharePoint).
  • Knowledge of medical terminology and clinical research concepts.
  • Ability to work independently and collaboratively in a team.
  • Problem-solving and analytical skills.
  • Familiarity with electronic case report form systems (e.g., Medidata Rave, Inform, TrialKit) preferred.
  • Ability to manage small projects and respond to urgent needs effectively.

Physical Requirements:
  • Ability to sit, stand, walk, reach with hands and arms, and use hands/fingers for handling or feeling.
  • Ability to lift and/or move up to 20 pounds.
  • Reasonable accommodation may be provided for individuals with disabilities.

Why JCCT?
JCCT has provided exceptional customer service to clients, volunteers, and vendors for the last 20 years. This team effort has resulted in our company getting recognized as one of the best clinical research sites in the United States.
We are actively growing through acquisition and organic growth and need high performing individuals to help support our continued success. Our clients come from all over the world to place a study at our research sites. We are proud of what we have accomplished and invite you to explore career opportunities with us. JCCT makes a promise to support, accept and respect you as an individual, in our family focused environment.
Our vision is to make a difference in our world to help improve the health and wellbeing of others through pharmaceutical research and the processes of drug development. Our impact is driven by genuine care, support and customer service provided to our employees, volunteers, and sponsors.
If you are looking for a positive work environment and the opportunity for personal growth and satisfaction, we encourage you to apply at JCCT. Qualified candidates will be contacted for interviews. Unleash your potential and apply today!
EEO
JCCT provides equal employment opportunities (EEO) to all employees and applicants. We value diversity at our company, and it is our policy to recruit, hire, and promote qualified individuals without regard to race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.
Salary Description
$25.00 per hour

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