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Clinical Research Associate Jobs in Riverside, CA

Bio-Rad Laboratories, Inc

Research Associate I

Irvine, CA · On-site

$70 - $77/hr

The position requires a working knowledge of laboratory experimentation, general chemistry, and clinical chemistry. As a Research Associate I, you will be working under the guidance of scientists to ...

Bio-Rad Laboratories, Inc.

Research Associate I

Irvine, CA · On-site

$70K - $77K/yr

The position requires a working knowledge of laboratory experimentation, general chemistry, and clinical chemistry. As a Research Associate I, you will be working under the guidance of scientists to ...

Bio-Rad Laboratories

Research Associate I

Irvine, CA

$70K - $77K/yr

The position requires a working knowledge of laboratory experimentation, general chemistry, and clinical chemistry. As a Research Associate I, you will be working under the guidance of scientists to ...

Bio-rad Laboratories, Inc.

Research Associate II

Irvine, CA · On-site

$70K - $95K/yr

The position requires a strong knowledge of laboratory experimentation, general chemistry, and clinical chemistry. As a Research Associate II, you will be working under the guidance of scientists to ...

Bio-Rad Laboratories

Research Associate II

Irvine, CA

$70K - $95K/yr

The position requires a strong knowledge of laboratory experimentation, general chemistry, and clinical chemistry. As a Research Associate II, you will be working under the guidance of scientists to ...

Bio-Rad Laboratories

Research Associate II

Irvine, CA · On-site

$70K - $95K/yr

The position requires a strong knowledge of laboratory experimentation, general chemistry, and clinical chemistry. As a Research Associate II, you will be working under the guidance of scientists to ...

Bio-Rad Laboratories

Research Associate I

Irvine, CA · On-site

$70K - $77K/yr

The position requires a working knowledge of laboratory experimentation, general chemistry, and clinical chemistry. As a Research Associate I, you will be working under the guidance of scientists to ...

Bio-Rad Laboratories, Inc.

Research Associate II

Irvine, CA · On-site

$70K - $95K/yr

The position requires a strong knowledge of laboratory experimentation, general chemistry, and clinical chemistry. As a Research Associate II, you will be working under the guidance of scientists to ...

Bio-rad Laboratories, Inc.

Research Associate I

Irvine, CA · On-site

$70K - $77K/yr

The position requires a working knowledge of laboratory experimentation, general chemistry, and clinical chemistry. As a Research Associate I, you will be working under the guidance of scientists to ...

City of Hope

Clin Research Nurse - BSN - OC

Irvine, CA · On-site

Work collaboratively with physicians, Clinical Research Associates (CRA) and pharmacists to coordinate care for an assigned population of patients who are enrolled in to IRB clinical research trials.

Medix

Clinical Research Coordinator

Murrieta, CA · On-site

$31 - $38/hr

Must have oncology clinical research experience * Minimum of two years of clinical research experience Preferred Skills * Bachelor's degree preferred, but not required * Clinical skills highly ...

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All JobsClinical Research Associate JobsClinical Research Associate Jobs in Riverside, CA

Clinical Research Associate information

See Riverside, CA salary details

$12

$42

$72

How much do clinical research associate jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for clinical research associate in Riverside, CA is $42.91, according to ZipRecruiter salary data. Most workers in this role earn between $30.10 and $54.90 per hour, depending on experience, location, and employer.

What is a clinical research associate?

Clinical Research Associates (CRAs) are professionals responsible for monitoring and overseeing clinical trials to ensure they are conducted in accordance with regulatory guidelines, protocols, and ethical standards. They play a key role in ensuring the safety of trial participants and the integrity of collected data. CRAs often visit clinical trial sites to verify data accuracy, maintain study documentation, and provide training to site staff. Their work ensures that new drugs, treatments, or medical devices are tested rigorously before they reach the market.

What are the key skills and qualifications needed to thrive as a clinical research associate?

To thrive as a Clinical Research Associate, you need a solid background in life sciences, attention to detail, and experience with clinical trial protocols, often supported by a relevant bachelor's degree. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and sometimes certifications like ACRP or SOCRA is typically required. Strong organizational, communication, and problem-solving skills help build effective relationships with research sites and ensure compliance. These skills are vital for maintaining the integrity of clinical trials, ensuring regulatory adherence, and advancing medical research efficiently.

What are some common challenges clinical research associates face when monitoring clinical trial sites?

Clinical Research Associates (CRAs) often encounter challenges such as ensuring protocol compliance across multiple sites, managing tight project timelines, and maintaining accurate documentation. Additionally, CRAs must effectively communicate with site staff to resolve issues and ensure data integrity, all while adhering to regulatory guidelines. Balancing frequent travel, adapting to different site environments, and handling unexpected issues such as patient recruitment delays are also typical aspects of the role.

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

AspectClinical Research AssociateClinical Trial Coordinator
CredentialsBachelor's degree, often with clinical research certificationsBachelor's degree, often with clinical research or healthcare certifications
Work EnvironmentMonitors clinical sites, reviews data, ensures complianceCoordinates trial activities, manages schedules, and communicates with sites
Employer & IndustryPharmaceutical companies, CROs, biotech firmsHospitals, research institutions, CROs

Both roles are essential in clinical trials, with CRAs focusing on site monitoring and compliance, while Clinical Trial Coordinators handle day-to-day trial management. They often collaborate but have distinct responsibilities within the clinical research process.

Is being a clinical research associate worth it?

A clinical research associate (CRA) monitors clinical trials to ensure compliance with protocols and regulations, often requiring strong organizational and communication skills. The role offers opportunities for career growth, competitive salaries, and work in the healthcare or pharmaceutical industries, but it can involve irregular hours and travel. Overall, it can be a rewarding career for those interested in medical research and patient safety.

Is it hard to get a clinical research associate 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 familiarity with trial management tools can improve job prospects, but entry-level roles may be easier to obtain with relevant internships or certifications.
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Clinical Research Associate jobs near you
Infographic showing various Clinical Research Associate job openings in Riverside, CA as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $89,243 per year, or $42.9 per hour.

Clinical Research Coordinator (Experienced) (Bilingual-Spanish) (Riverside)

Irvine Clinical Research

Riverside, CA

$66K - $80K/yr

Full-time

Medical, Dental, Vision, PTO

Re-posted 3 days ago

Job description

Riverside Clinical is part of the Irvine Clinical Research site network, the largest of its kind on the West Coast. With 5 research centers in California, we are leaders in the search for new treatments in neurology, psychiatry, and obesity medicine. Our largest area of research is in Alzheimer's Disease prevention and treatment drug trials, and our doctors were the largest contributors in the world to the most recently FDA-approved medication in Alzheimer's Disease.
 
In this role, we are seeking CRCs with proven trial experience. Ideally, candidates will have worked as a primary coordinator on complex drug trial and have exceeded enrollment targets while producing quality work. Furthermore, we are seeking a bilingual (Spanish) professional to better serve our community.
Job Duties
  • Manage daily operations for assigned clinical trial projects
  • Perform study procedures in accordance with GCP and study protocols
  • Organize and maintain study data in a complete and correct manner in CRIO eSource/CTMS
  • Cultivate enthusiastic and professional relationships with patients and sponsors alike
  • Work closely with recruitment and prescreening teams to meet study enrollment goals
  • Conduct diagnostic, efficacy, and safety assessments as needed
Job Requirements
  • Bachelor's degree or higher
  • One (1) or more years of clinical research coordinator experience
  • Attention to detail and the ability to handle multiple tasks with precision
  • Demonstrated ability to work accurately and quickly with CTMS and eSource
  • A command of professional spoken and written English
  • A command of professional spoken and written Spanish
$66,560 - $80,000 a year
Hours and Compensation
This is a full-time employment position based in-person at our clinic on Central Avenue across the street from the Riverside Plaza mall. It is one stoplight away from the 91 freeway, and there is lots of free parking on-site, which can make for a convenient commute. We have five clinics throughout California, and this is our only one in the Inland Empire.
 
The estimated salary for this position is between $66k-$80k per year, depending on experience and education.
 
The company pays for 100% of health/dental/vision individual insurance costs for eligible full-time employees. Vacation (PTO) is earned at a rate of 3 weeks per year.
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