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Clinical Trials Protocol Administrator Jobs in Riverside, CA

Diality Inc

Clinical Research Associate

Irvine, CA · On-site

$120K - $135K/yr

... clinical trials in compliance with applicable regulations (e.g., FDA, ISO 14155, ICH-GCP). This ... Monitor site performance and compliance with protocols, regulations, and study timelines. * Support ...

Diality

Clinical Research Associate

Irvine, CA · Remote

$120K - $135K/yr

... clinical trials in compliance with applicable regulations (e.g., FDA, ISO 14155, ICH-GCP). This ... Monitor site performance and compliance with protocols, regulations, and study timelines. * Support ...

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All JobsClinical Trials Protocol Administrator JobsClinical Trials Protocol Administrator Jobs in Riverside, CA

Clinical Trials Protocol Administrator information

See Riverside, CA salary details

$18

$28

$46

How much do clinical trials protocol administrator jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for clinical trials protocol administrator in Riverside, CA is $28.85, according to ZipRecruiter salary data. Most workers in this role earn between $23.85 and $31.11 per hour, depending on experience, location, and employer.

What does a clinical trials protocol administrator do?

A Clinical Trials Protocol Administrator is responsible for coordinating and managing the documentation and logistics related to clinical trial protocols. Their role involves ensuring that all trial procedures comply with regulatory and ethical standards, maintaining accurate records, and facilitating communication between research teams, sponsors, and regulatory bodies. They play a crucial role in starting, monitoring, and closing clinical studies, helping to ensure that protocols are followed and that trials run smoothly.

What are the key skills and qualifications needed to thrive as a clinical trials protocol administrator, and why are they important?

To excel as a Clinical Trials Protocol Administrator, you need a solid background in clinical research, regulatory compliance, and protocol development, often supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and certifications like Certified Clinical Research Professional (CCRP) are highly beneficial. Strong organizational skills, attention to detail, and effective communication help manage complex documentation and coordinate with multiple stakeholders. These capabilities are crucial for ensuring protocol adherence, data integrity, and the smooth execution of clinical trials.

What are some common challenges faced by clinical trials protocol administrators, and how can they be managed?

Clinical Trials Protocol Administrators often face challenges such as coordinating multiple stakeholders, managing strict regulatory compliance, and maintaining accurate documentation. Balancing the needs of investigators, sponsors, and regulatory bodies requires strong organizational and communication skills. To manage these challenges, administrators typically use project management tools, stay updated on regulations, and establish clear communication channels within the clinical research team. Proactively addressing issues and maintaining detailed records can help ensure trials run smoothly and meet compliance standards.

What is the difference between Clinical Trials Protocol Administrator vs Clinical Research Coordinator?

AspectClinical Trials Protocol AdministratorClinical Research Coordinator
Primary ResponsibilitiesDevelops, reviews, and manages trial protocols, ensuring compliance and accuracyCoordinates daily trial activities, enrolls participants, and collects data
Required CredentialsBachelor's degree in health sciences or related field; certifications like CCRP are commonBachelor's degree in health sciences or related field; often requires clinical research certifications
Work EnvironmentOffice-based, regulatory and administrative settingsClinical sites, hospitals, or research facilities
Industry UsageUsed across pharmaceutical, biotech, and academic research organizationsPrimarily in hospitals, clinics, and research institutions

While both roles support clinical trials, the Clinical Trials Protocol Administrator focuses on protocol development and compliance, whereas the Clinical Research Coordinator handles participant management and daily trial operations.

What job categories do people searching Clinical Trials Protocol Administrator jobs in Riverside, CA look for?

The top searched job categories for Clinical Trials Protocol Administrator jobs in Riverside, CA are:

What cities near Riverside, CA are hiring for Clinical Trials Protocol Administrator jobs?

Cities near Riverside, CA with the most Clinical Trials Protocol Administrator job openings:

Clinical Trials Protocol Administrator jobs near you
Infographic showing various Clinical Trials Protocol Administrator job openings in Riverside, CA as of June 2026, with employment types broken down into 72% Full Time, 20% Part Time, 4% Temporary, and 4% Contract. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution, with an average salary of $60,008 per year, or $28.9 per hour.

Sub-Investigator (NP or PA) (Bilingual-Spanish) (Riverside)

Irvine Clinical Research

Riverside, CA • On-site

$125K - $130K/yr

Full-time

Medical, Dental, Vision, PTO

This job post has expired today. Applications are no longer accepted.

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.

Riverside Clinical is hiring a clinician who is an NP or PA. The clinician will oversee clinical trials of some of the most promising drugs under investigation in Alzheimer's Disease treatment and prevention.
Job Duties
  • Manage study team as a Sub-Investigator, ensuring trials are conducted safely and per protocol
  • Conduct clinical intake interviews to determine medical eligibility of potential study participants
  • Manage the safety of study participants; respond appropriately to adverse events in a timely manner
  • Perform and oversee infusion, phlebotomy, physical exams, and other assessments
  • Work closely with our team of doctors and study coordinators
Job Requirements
  • Valid license to practice in California as an NP or PA-C, free and unencumbered
  • Experience working with older adults in a clinical or research setting
  • Clinical research experience is preferred, but not required
  • A command of professional spoken and written English
  • A command of professional spoken and written Spanish
$125,000 - $130,000 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.

There are no planned overnight or weekend hours.

The starting salary for this position is indicated above. Higher salary is available with candidates who are current/previous sub-investigators in pharmaceutical clinical trials of Alzheimer's Disease.

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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