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Research Coordinator I Jobs in Riverside, CA (NOW HIRING)

Report AEs promptly; report SAEs to sponsor within 24 hours and notify PI/Sub-I/supervisor ... Must have oncology clinical research experience * Minimum of two years of clinical research ...

As a Procurement Transplant Coordinator, you will provide primary medical care to authorized organ ... research at the time of recovery. The PTC-I directs the medical treatment regimen to meet the ...

Transplant Coordinator 1

Redlands, CA · On-site

$84K - $108K/yr

As a Procurement Transplant Coordinator, you will provide primary medical care to authorized organ ... research at the time of recovery. The PTC-I directs the medical treatment regimen to meet the ...

As a Procurement Transplant Coordinator, you will provide primary medical care to authorized organ ... research at the time of recovery. The PTC-I directs the medical treatment regimen to meet the ...

As a Procurement Transplant Coordinator, you will provide primary medical care to authorized organ ... research at the time of recovery. The PTC-I directs the medical treatment regimen to meet the ...

Research and problem-solving capabilities, including the ability to identify discrepancies and escalate issues appropriately. * Ability to follow established policies, procedures, and credit/funding ...

Research Chemist

Jurupa Valley, CA · On-site

$70K - $80K/yr

Support the Laboratory Manager and Project Coordinator in daily Central Laboratory operations ... Well-versed in Microsoft Office applications (i.e., Outlook, Word, Excel, SharePoint, and Planner)

Research Chemist

Jurupa Valley, CA · On-site

$70K - $80K/yr

Support the Laboratory Manager and Project Coordinator in daily Central Laboratory operations ... Well-versed in Microsoft Office applications (i.e., Outlook, Word, Excel, SharePoint, and Planner)

Support the Laboratory Manager and Project Coordinator in daily Central Laboratory operations ... Well-versed in Microsoft Office applications (i.e., Outlook, Word, Excel, SharePoint, and Planner)

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Showing results 1-20

Research Coordinator I information

See Riverside, CA salary details

$22.4K

$84.1K

$117.4K

How much do research coordinator i jobs pay per year?

As of Aug 27, 2026, the average yearly pay for research coordinator i in Riverside, CA is $84,056.00, according to ZipRecruiter salary data. Most workers in this role earn between $63,600.00 and $103,800.00 per year, depending on experience, location, and employer.

What does a Research Coordinator I do?

A Research Coordinator I is responsible for supporting the planning, implementation, and management of research studies, typically in academic, medical, or clinical settings. Their duties often include recruiting and screening study participants, collecting and managing data, ensuring compliance with regulatory requirements, and coordinating communication among research team members. They also help prepare study materials, maintain accurate records, and support reporting and analysis. This entry-level role is essential for ensuring research projects run smoothly and meet ethical and procedural standards.

What are the key skills and qualifications needed to thrive as a Research Coordinator I, and why are they important?

To thrive as a Research Coordinator I, you need a bachelor’s degree in a relevant field, a solid understanding of research methodologies, and experience with data collection and management. Familiarity with regulatory compliance tools, clinical trial management systems, and platforms like REDCap is highly valued. Strong organizational skills, attention to detail, and clear communication are essential soft skills for coordinating studies and supporting research teams. These abilities ensure accurate study execution, regulatory compliance, and effective collaboration, which are critical for research success.

What are the most common challenges faced by a Research Coordinator I when managing multiple studies simultaneously?

As a Research Coordinator I, juggling several studies at once often means balancing competing deadlines, ensuring regulatory compliance, and maintaining accurate documentation for each project. Effective time management and clear communication with both research teams and participants are essential to prevent errors and delays. Adapting to shifting priorities and being proactive in resolving logistical issues are also key skills that help coordinators maintain study integrity and project timelines.

What is the difference between Research Coordinator I vs Research Coordinator II?

AspectResearch Coordinator IResearch Coordinator II
QualificationsBachelor's degree often required; entry-level experienceSimilar or slightly more experience; may require additional certifications
ResponsibilitiesAssists with data collection, participant coordination, and basic research tasksHandles more complex data analysis, protocol adherence, and oversight
Work EnvironmentClinical or research settings, supervised tasksSame environment, with increased independence
Usage in IndustryCommon entry-level role in research projectsMid-level role with more responsibilities

The main difference between Research Coordinator I and Research Coordinator II lies in experience and responsibility level. Research Coordinator I typically performs foundational tasks under supervision, while Research Coordinator II handles more complex duties with greater independence. Both roles are essential in research settings, with the II position often requiring additional experience or certifications.

What are the most commonly searched types of Research I jobs in Riverside, CA?

The most popular types of Research I jobs in Riverside, CA are:

What cities near Riverside, CA are hiring for Research Coordinator I jobs?

Cities near Riverside, CA with the most Research Coordinator I job openings:

Infographic showing various Research Coordinator I job openings in Riverside, CA as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 14% Part Time, and 2% Contract. Highlights an 77% Physical, 4% Hybrid, and 19% Remote job distribution, with an average salary of $84,056 per year, or $40.4 per hour.

Senior Clinical Research Coordinator

Lake Forest, CA • On-site

Orange County Research Center
Health Care and Social Assistance • 11 - 50 employees

$25.50 - $34/hr

Other

Posted 4 days ago


Job description

Company Description Orange County Research Center is a premier clinical research facility specializing in Phase I–IV clinical trials across diverse therapeutic areas. With decades of experience and a state-of-the-art Phase I unit, the center supports sponsors and CROs in conducting high-quality, compliant, and efficient studies. A multidisciplinary team collaborates to ensure robust study design, accurate data collection, and timely execution. The organization is dedicated to scientific excellence, participant safety, and operational integrity, advancing innovative therapies that improve patient outcomes. Team members join a mission-driven environment focused on rigorous research and meaningful clinical impact.
Role Description The Senior Clinical Research Coordinator is a full-time, on-site role based in Lake Forest, CA. This position oversees the planning, coordination, and execution of clinical trials, including participant screening, enrollment, and follow-up visits according to study protocols. Day-to-day responsibilities include managing informed consent processes, maintaining source documentation and regulatory binders, scheduling and conducting study procedures, and ensuring protocol adherence. The coordinator collaborates closely with investigators, sponsors, and internal teams to support monitoring visits, resolve queries, and maintain data accuracy and timeliness. The role also involves training junior staff, supporting quality assurance activities, and promoting best practices in participant safety and compliance.
Qualifications
  • Demonstrated clinical research experience with involvement in Clinical Trials and strong Research skills.
  • Proficiency in managing Informed Consent processes, including educating participants and ensuring proper documentation.
  • Experience interpreting and implementing study Protocols with attention to regulatory and ethical requirements.
  • Knowledge of Good Clinical Practice (GCP), ICH guidelines, and applicable FDA and IRB regulations.
  • Strong organizational, time-management, and documentation skills, with high attention to detail.
  • Effective written and verbal communication skills and ability to collaborate with multidisciplinary teams.
  • Prior experience as a Clinical Research Coordinator, preferably in Phase I–IV trials; senior or lead experience is highly desirable.
  • Associate or Bachelor’s degree in a health-related field or equivalent experience; professional certification in clinical research (e.g., ACRP, SOCRA) is a plus.
  • Ability to work on-site in Lake Forest, CA, including occasional extended hours to support study needs.