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Medical Research Associate Jobs in Riverside, CA

This associate will play a critical role in the creation and delivery of accurate, high-quality ... Collaborate closely with internal cross-functional teams (Clinical, Biostatistics, Medical Affairs ...

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Medical Research Associate information

See Riverside, CA salary details

$39.1K

$55.6K

$61K

How much do medical research associate jobs pay per year?

As of Jun 12, 2026, the average yearly pay for medical research associate in Riverside, CA is $55,634.00, according to ZipRecruiter salary data. Most workers in this role earn between $56,300.00 and $60,500.00 per year, depending on experience, location, and employer.

How hard is it to get a CRA job?

Securing a Clinical Research Associate (CRA) position can be competitive, often requiring a relevant degree in life sciences or healthcare, along with experience in clinical trials. Strong organizational skills, knowledge of Good Clinical Practice (GCP), and certification such as CCRP can improve chances, but entry may be challenging for those without related experience or training.

How much does a CRC make?

A Clinical Research Coordinator (CRC) in Houston typically earns between $50,000 and $70,000 annually, depending on experience, certifications, and the employer. Salaries can vary based on the complexity of trials and the research environment.

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.

Can you be a CRA with no experience?

A Clinical Research Associate (CRA) typically requires prior experience in clinical trials or related healthcare fields, as the role involves monitoring study sites and ensuring compliance. Entry-level positions may be available for those with relevant educational backgrounds, strong organizational skills, and knowledge of Good Clinical Practice (GCP) guidelines, but most employers prefer candidates with some related experience or training. Certifications such as the CCRP can also enhance prospects for those new to the field.

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 may require knowledge of Good Clinical Practice (GCP) guidelines. The role typically involves detailed documentation and adherence to regulatory standards.
What are the most commonly searched types of Medical Research jobs in Riverside, CA? The most popular types of Medical Research jobs in Riverside, CA are:
What are popular job titles related to Medical Research Associate jobs in Riverside, CA? For Medical Research Associate jobs in Riverside, CA, the most frequently searched job titles are:
What job categories do people searching Medical Research Associate jobs in Riverside, CA look for? The top searched job categories for Medical Research Associate jobs in Riverside, CA are:
What cities near Riverside, CA are hiring for Medical Research Associate jobs? Cities near Riverside, CA with the most Medical Research Associate job openings:
Infographic showing various Medical Research Associate job openings in Riverside, CA as of June 2026, with employment types broken down into 45% Full Time, 32% Part Time, and 23% Contract. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $55,634 per year, or $26.7 per hour.
Clinical Research Associate - Irvine, CA

Clinical Research Associate - Irvine, CA

MDxHealth

Irvine, CA • On-site

$64K - $75K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 12 days ago


Job description

The Clinical Research Associate (CRA) assists the Clinical Affairs Team in the administration of clinical research studies. The CRA will respond to a variety of study account inquiries, issues and requests and act as a liaison between the lab and the study account. The CRA will monitor specimen TAT, set up new study accounts, manage current study accounts, requests, and track specimens, and ensure that all study specimens are adhering to the SOP. The CRA will work independently to monitor your study sites, including evaluation, initiation, routine and close out visits. The CRA will manage multiple aspects of subject’s welfare, including submission of protocol, consent documents for ethics/IRB approval and assist in the preparation of regulatory submissions as requested. The CRA will monitor clinical study data for completeness and accuracy, perform data cleaning, reconciliation of data queries and generate data reports as needed. When required, the CRA will perform remote or on-site data mining in medical office EMR systems. Provide administrative support as needed to execute clinical study start up and close out duties. Provide assistance to study sites with respect to communication, study supplies, etc. Maintain close communication with the Director, Clinical Affairs, while taking initiative and working independently on assigned tasks.

  • Location – Irvine, CA. This is a hybrid position – at least 3 days in the office.
  • Basic knowledge of biology, genomics, or molecular biology.
  • Minimum of at least 1 year of study experience as a CRA, including at least 1 year of active independent field monitoring experience as a CRA— all types of visits.
  • Experience with data mining, data review and data management.
  • Strong problem-solving skills and ability to work independently.
  • Self-motivated, detail-oriented, organized, and able to prioritize and manage multiple projects requirements simultaneously.
  • Willingness to travel nationally 50% of the time or as needed.
  • Hiring range: $64,500 to $75,000 annually. The actual rate will be determined based on experience and other factors permitted by law.
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MDxHealth seeks talented people who are passionate about improving the diagnosis and treatment of cancer patients.

MDxHealth is building world class healthcare company, providing significant career development and financial opportunities.

Company Benefits:

We offer a comprehensive compensation and benefits package, which includes a competitive salary, company paid medical, dental, vision and life insurance coverage, 401(k) with company match, generous employee discounts, a casual, but driven work environment, and the ability to make a real difference as a key contributor to our growth.

MDxHealth is 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, or protected veteran status and will not be discriminated against on the basis of disability.

Accessibility: If you need an accommodation as part of the employment process, please contact Human Resources at: 866-259-5644.