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Medical Research Associate Jobs (NOW HIRING)

The research associate will assist in coordinating day-to-day activities associated with clinical ... Review the medical record to assess eligibility based on defined criteria. * Recruit patients and ...

Research Associate

Santa Ana, CA · On-site

$28.82 - $36.25/hr

The Research Associate will join the team under the general oversight of the Orange County TB ... Coordinate participant screening and recruitment activities, including review of medical records ...

The Hemond Lab ( at the University of Massachusetts Chan Medical School ( is seeking a Research Associate for investigations of human, in-vivo MRI biomarker development, assessment and translation ...

Research Associate Location: West Salem, Wisconsin Come grow with DLF! At DLF, we're passionate ... A valid driver's license with a good driving record, plus the ability to obtain a DOT medical card ...

Research Associate Location: West Salem, Wisconsin Come grow with DLF! At DLF, we're passionate ... A valid driver's license with a good driving record, plus the ability to obtain a DOT medical card ...

Job Title Research Associate Agency Texas A&M Agrilife Research Department Amarillo Proposed ... Texas A&M Veterinary Medical Diagnostic Laboratory As the nation's largest most comprehensive ...

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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 22, 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:
Infographic showing various Medical Research Associate job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 69% Full Time, 28% Part Time, 1% Temporary, and 1% Contract. 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.
Research Associate

Research Associate

Trinity Health

Muskegon, MI • On-site

Full-time

Posted 6 days ago


Job description

Employment Type:
Full timeShift:
Day Shift
Description:
Highlights:
  • This position is full time (40 hours/week), term-limited and contingent upon grant funding continuation and successful patient recruitment.
  • Great opportunity to gain research experience.
  • Focused on maternal and child health outcomes.

Position summary:
We are seeking an ambitious, enthusiastic research associate to join our growing team. In this role you will interface with research participants to recruit, assess eligibility criteria, determine subject availability, assist investigators with obtaining informed consent, perform follow up data collection and enter into the database. The research associate will assist in coordinating day-to-day activities associated with clinical research study independently and under the direction of senior research staff and principal investigators to ensure that the objectives of an established research protocol are met and in compliance within IRB and sponsor guidelines.
What the Research Associate will do:
  • Monitor obstetrical clinic schedules to screen for potential participants.
  • Review the medical record to assess eligibility based on defined criteria.
  • Recruit patients and obtain informed consent to Mission and Department standards. Consenting process includes the ability to do phone calls, e-consent, or in-person.
  • Conduct research surveys and other protocol activities.
  • Enter, clean, and manage research data.

Minimum qualifications:
  • Bachelor's degree in a related science, healthcare or business field or the equivalent combination of education and experience.
  • Ability to work some flexible hours to accommodate study and patient schedules is required.
  • Ability to work independently & with high accountability, and ability to work in team settings.
  • Excellent writing and interpersonal communication skills.
  • Professional, calm, and compassionate demeanor in the presence of injured and stressed patients and families.

Our Commitment
Rooted in our Mission and Core Values, we honor the dignity of every person and recognize the unique perspectives, experiences, and talents each colleague brings. By finding common ground and embracing our differences, we grow stronger together and deliver more compassionate, person-centered care. We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other status protected by federal, state, or local law.

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About Trinity Health

Sourced by ZipRecruiter

Trinity Health Ann Arbor is a 537 -bed teaching hospital located on 340 acre campus. Recognized by IBM Watson as a Top 100 Hospital and #1 Teaching Hospital, Trinity Health Ann Arbor has been a leading health care provider for more than 100 years. Trinity Health has received numerous local and national awards in recognition of our leadership, quality outcomes, and clinical excellence.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Livonia, MI, US