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Clinical Trial Jobs in Riverside, CA (NOW HIRING)

CYNET SYSTEMS

Associate Clinical Research Specialist

Irvine, CA · On-site

$38 - $43/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Trial Master File (TMF) management. * Good Documentation Practices. * Clinical Trial Management System (CTMS). * Electronic Data Capture (EDC). * Problem-solving and critical thinking skills.

Jj

Clinical Research Leader

Irvine, CA · On-site

  • PTO

Develop clinical trial documents (e.g. study protocol, informed consents, CRF, monitoring plan, study manual, investigator brochure, annual reports) with minimal direction. * Ensure trial ...

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All JobsClinical Trial JobsClinical Trial Jobs in Riverside, CA

Clinical Trial information

See Riverside, CA salary details

$30

$65

$100

How much do clinical trial jobs pay per hour?

As of Aug 15, 2026, the average hourly pay for clinical trial in Riverside, CA is $65.22, according to ZipRecruiter salary data. Most workers in this role earn between $52.93 and $73.46 per hour, depending on experience, location, and employer.

What are clinical trials?

Clinical trials are research studies that involve human participants and are designed to evaluate the safety and effectiveness of new medical treatments, drugs, or devices. These trials follow a carefully controlled protocol and are conducted in phases to systematically assess outcomes. Participants may include patients with specific medical conditions or healthy volunteers, depending on the study's goals. The results from clinical trials help inform medical decisions and regulatory approvals for new therapies.

What are the key skills and qualifications needed to thrive in a clinical trial role?

To thrive in a Clinical Trial role, you need a solid understanding of clinical research principles, regulatory compliance, and data management, usually supported by a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) certification, and clinical trial management software is typically required. Strong attention to detail, organizational abilities, and effective communication skills help professionals coordinate complex processes and collaborate with interdisciplinary teams. These competencies are vital to ensure trials are conducted ethically, efficiently, and in compliance with regulatory standards.

What jobs are there in clinical trials?

Jobs in clinical trials include clinical research coordinators, clinical research associates, data managers, regulatory affairs specialists, and study nurses. These roles involve tasks such as patient recruitment, data collection, monitoring trial progress, and ensuring compliance with regulations, often requiring knowledge of Good Clinical Practice (GCP) and relevant certifications. The work environment is typically a research site, hospital, or pharmaceutical company, with schedules varying from standard to flexible hours depending on the role.

What are some common challenges faced by professionals working in clinical trial management, and how can they be addressed?

Professionals in clinical trial management often encounter challenges such as adhering to strict regulatory requirements, managing complex timelines, and ensuring effective communication among multidisciplinary teams. Overcoming these challenges typically involves thorough planning, continuous training on regulatory updates, and the use of project management tools to track progress and coordinate tasks. Building strong relationships with investigators and fostering open communication can also help address issues quickly and maintain trial integrity.

How to get into a clinical trial career?

A career in clinical trials typically requires a background in healthcare, life sciences, or related fields, along with knowledge of Good Clinical Practice (GCP) guidelines. Entry-level roles often require a bachelor's degree, and certifications such as the Certified Clinical Research Professional (CCRP) can enhance job prospects. Gaining experience through internships or entry-level positions in research settings is also beneficial.

What are the most commonly searched types of Clinical Trial jobs in Riverside, CA?

The most popular types of Clinical Trial jobs in Riverside, CA are:

What are popular job titles related to Clinical Trial jobs in Riverside, CA?

For Clinical Trial jobs in Riverside, CA, the most frequently searched job titles are:

What job categories do people searching Clinical Trial jobs in Riverside, CA look for?

The top searched job categories for Clinical Trial jobs in Riverside, CA are:

What cities near Riverside, CA are hiring for Clinical Trial jobs?

Cities near Riverside, CA with the most Clinical Trial job openings:

Clinical Trial jobs near you
Infographic showing various Clinical Trial job openings in Riverside, CA as of August 2026, with employment types broken down into 2% As Needed, 73% Full Time, 17% Part Time, and 8% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $135,661 per year, or $65.2 per hour.

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

Irvine Clinical Research

Riverside, CA

$66K - $80K/yr

Full-time

Re-posted 13 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
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.