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Medical Research Associate Jobs (NOW HIRING)

ICON

Senior Medical Research Associate

Lenexa, KS · On-site

Senior Medical Research Associate (Paramedic) - Lenexa, KS (Onsite) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and ...

Virginia Tech

Research Associate

Blacksburg, VA · On-site

Research Associate Apply now Back to search results Job no: 534727 Work type: Research Faculty ... in medical research. Required Qualifications Graduate degree in biology, health sciences ...

R&D Partners

Research Associate II

Tucson, AZ · On-site

$27/hr

R&D Partners is seeking to hire a Research Associate II in Tucson, AZ . Your main responsibilities ... Medical insurance - PPO, HMO & * Dental & Vision insurance * 401k plan * Employee Assistance ...

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All JobsMedical Research Associate Jobs

Medical Research Associate information

See salary details

$37.5K

$53.3K

$58.5K

How much do medical research associate jobs pay per year?

As of Jul 1, 2026, the average yearly pay for medical research associate in the United States is $53,326.00, according to ZipRecruiter salary data. Most workers in this role earn between $54,000.00 and $58,000.00 per year, depending on experience, location, and employer.

What qualifications do you need to be a research associate?

A research associate in the medical field typically needs at least a bachelor's degree in a related science or healthcare discipline, such as biology, chemistry, or nursing. Relevant skills include data analysis, laboratory techniques, and familiarity with research protocols; some positions may require a master's degree or higher. Certifications like Good Clinical Practice (GCP) or Good Laboratory Practice (GLP) can also be advantageous.

Is it hard to get a CRA job?

Securing a Clinical Research Associate (CRA) position can be competitive, often requiring relevant experience, a degree in life sciences or related fields, and knowledge of Good Clinical Practice (GCP) guidelines. Entry-level roles may be easier to obtain with strong educational backgrounds and certifications like the CCRP, but advancing to senior CRA positions typically demands proven experience in clinical trials and monitoring skills.

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

AspectMedical Research AssociateClinical Research Coordinator
CredentialsBachelor’s degree in life sciences or related field; certifications like CCRP are commonBachelor’s degree in health sciences, nursing, or related; often holds certifications like CCRP or CCRC
Work EnvironmentResearch labs, pharmaceutical companies, academic institutionsHospitals, clinics, research sites
Employer & IndustryPharmaceutical companies, biotech firms, academic research centersHospitals, clinical trial sites, research organizations
Common Search & ComparisonMedical Research Associate vs Clinical Research Coordinator

Both roles involve coordinating and supporting clinical research, but Medical Research Associates typically focus on data collection, analysis, and supporting laboratory work, while Clinical Research Coordinators manage patient recruitment, scheduling, and regulatory compliance at research sites. The roles often overlap, but their primary responsibilities and work environments differ slightly.

Is CRA better than CRC?

A Clinical Research Associate (CRA) and a Clinical Research Coordinator (CRC) are both key roles in clinical trials, but they have different responsibilities. CRAs typically oversee multiple sites, monitor trial progress, and ensure compliance, often working remotely or traveling frequently, while CRCs manage day-to-day trial activities at a specific site, including patient recruitment and data collection. Both roles require knowledge of Good Clinical Practice (GCP) and relevant certifications, but CRAs usually have more experience and may require a background in monitoring or regulatory aspects.

What are the key skills and qualifications needed to thrive as a Medical Research Associate, and why are they important?

To thrive as a Medical Research Associate, you need a strong background in life sciences, data analysis, and clinical research methods, often supported by a relevant degree such as biology or pharmacology. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) certification, and statistical analysis software is typically required. Attention to detail, critical thinking, and effective communication are standout soft skills for this role. These abilities ensure accuracy, regulatory compliance, and successful collaboration in conducting and managing clinical studies.

What are some common challenges faced by Medical Research Associates when coordinating clinical trials?

Medical Research Associates often encounter challenges such as managing tight timelines, ensuring strict adherence to regulatory guidelines, and maintaining clear communication among diverse teams. Coordinating with investigators, sponsors, and regulatory bodies requires strong organizational and interpersonal skills. Additionally, balancing multiple studies simultaneously can be demanding, making effective time management and attention to detail essential for success in this role.

What are Medical Research Associates?

Medical Research Associates are professionals who assist in the planning, coordination, and execution of clinical trials and medical research studies. They ensure that studies comply with regulatory guidelines and ethical standards, collect and analyze data, and help prepare reports for publication. Their work is essential in advancing medical knowledge and supporting the development of new treatments and therapies.

What does a medical research associate do?

A medical research associate (MRA) supports clinical trials by coordinating study activities, ensuring compliance with protocols, collecting and managing data, and monitoring patient safety. They often work closely with investigators, use data management tools, and require knowledge of Good Clinical Practice (GCP) standards. The role typically involves documentation, communication, and adherence to regulatory requirements.
More about Medical Research Associate jobs
What cities are hiring for Medical Research Associate jobs? Cities with the most Medical Research Associate job openings:
What are the most commonly searched types of Medical Research jobs? The most popular types of Medical Research jobs are:
What states have the most Medical Research Associate jobs? States with the most job openings for Medical Research Associate jobs include:
What job categories do people searching Medical Research Associate jobs look for? The top searched job categories for Medical Research Associate jobs are:
Medical Research Associate jobs near you
Infographic showing various Medical Research Associate job openings in the United States as of June 2026, with employment types broken down into 91% Full Time, and 9% Part Time. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $53,326 per year, or $25.6 per hour.
Senior Medical Research Associate

Senior Medical Research Associate

ICON

Lenexa, KS • On-site

Part-time

Medical, Dental, Vision, Life, Retirement

Posted 6 days ago

Job description

Senior Medical Research Associate (Paramedic) - Lenexa, KS (Onsite)
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.
Paramedic - PRN
Note: The internal title for a licensed paramedic at ICON is Senior Research Associate. Further details below.
ICON plc is a world-leading clinical research organization. We advance clinical research by providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organizations.
With our patients at the center of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life.
The Role:
Our full-service clinic in Lenexa, Kansas, is a 114-bed, state-of-the-art research center, located near metropolitan Kansas City.
We are seeking a (PRN) Senior Medical Research Associate with active Paramedic licensure to support clinical research studies at our Lenexa, Kansas (KS) clinic.
Whether you're exploring a career in clinical research or already have experience in the field, this role offers a chance to contribute to work that supports the future of healthcare and disease management. Paramedic candidates without research experience are encouraged to apply.
Key Responsibilities
The Senior Medical Research Associate opportunity blends patient care with research responsibilities.
Clinical & Paramedic Responsibilities
  • Provide direct patient care within the onsite clinic, including advanced assessment, triage, vital signs, and urgent clinical support.
  • Perform Paramedic-level procedures within licensure scope, including IV placement, blood draws, specimen collection, injections, wound care, and emergency response/stabilization.
  • Monitor participant safety during research procedures and respond promptly to medical concerns, adverse events, or unexpected clinical situations.
  • Ensure medical equipment, supplies, and emergency materials are maintained, stocked, and fully operational.

Research & Operational Responsibilities
  • Assist in planning, coordinating, and executing clinical research activities in alignment with study protocols and regulatory requirements.
  • Support study visit procedures, including sample handling, documentation, timing, and protocol-driven tasks.
  • Conduct or support staff training, reinforce protocol adherence, and provide ongoing operational assistance to investigators and team members.
  • Track study progress, maintain accurate and audit-ready documentation, and ensure high-quality records throughout the study lifecycle.
  • Contribute to the development and review of study materials, including source documents, manuals, logs, and operational tools.

Qualifications
  • Active, unrestricted Paramedic state license.
  • National Registry Paramedic (NRP) certification or state-recognized equivalent.
  • Strong understanding of patient assessment, emergency response protocols, and clinical documentation standards.

#LI-KM3
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 request here.
Are you a current ICON Employee? Please click here to apply

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