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Clinical Research Data Assistant Jobs in Riverside, CA

Clinical Research Specialist Hybrid - onsite every Monday, Wednesday, and every other Friday Pay ... Assists in clinical data review to prepare data for statistical analyses and publications; * May ...

Research Assistant

Murrieta, CA · On-site

$21 - $32/hr

Valkyrie Clinical Trials (VCT) , a Flourish Research Company, is a leading Oncology multi-site ... Document assessments and study data per regs/GCP * Obtain and document informed consent following ...

Research Assistant

Murrieta, CA · On-site

$21 - $32/hr

Valkyrie Clinical Trials (VCT) , a Flourish Research Company, is a leading Oncology multi-site ... Document assessments and study data per regs/GCP * Obtain and document informed consent following ...

Research Assistant

Murrieta, CA · On-site

$21 - $32/hr

Valkyrie Clinical Trials (VCT) , a Flourish Research Company, is a leading Oncology multi-site ... Document assessments and study data per regs/GCP * Obtain and document informed consent following ...

Ensure quality data management activities - i.e., data review, query generation and resolution ... * Assist field clinical monitors in preparation for site training and monitoring visits * Support ...

Clinical Development & Research - Non-MD Job Category: Scientific/Technology All Job Posting ... Analyze and interpret clinical data; effectively communicate data using well-structured tables and ...

Showing results 21-40

Clinical Research Data Assistant information

See Riverside, CA salary details

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How much do clinical research data assistant jobs pay per hour?

As of Aug 15, 2026, the average hourly pay for clinical research data assistant in Riverside, CA is $23.69, according to ZipRecruiter salary data. Most workers in this role earn between $18.08 and $27.07 per hour, depending on experience, location, and employer.

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

To thrive as a Clinical Research Data Assistant, you need strong attention to detail, data entry accuracy, familiarity with clinical research protocols, and typically an associate’s or bachelor’s degree in a health-related or scientific field. Proficiency in data management systems such as REDCap, EDC platforms, and Microsoft Excel, as well as knowledge of Good Clinical Practice (GCP) guidelines, is often required. Strong organizational skills, clear communication, and the ability to collaborate with research teams make candidates stand out. These skills ensure careful handling of sensitive data, regulatory compliance, and efficient support for clinical research studies.

What does a clinical research data assistant do?

A Clinical Research Data Assistant is responsible for managing and organizing data collected during clinical trials and research studies. They ensure the accuracy, integrity, and confidentiality of data by entering, verifying, and maintaining research records. These professionals also assist with data cleaning, preparing reports, and supporting regulatory compliance. Their work is essential for the successful analysis and reporting of clinical research findings.

What are some typical challenges faced by clinical research data assistants in maintaining data accuracy?

Clinical Research Data Assistants often encounter challenges such as managing large volumes of complex data, ensuring accurate data entry from multiple sources, and adhering to strict regulatory standards. Mistakes can occur if data is not consistently verified or if communication between research teams is lacking, so attention to detail and strong organizational skills are essential. Regular audits, clear documentation procedures, and collaboration with clinical coordinators help address these challenges and maintain data integrity throughout the research process.

What is the difference between Clinical Research Data Assistant vs Clinical Research Coordinator?

AspectClinical Research Data AssistantClinical Research Coordinator
CredentialsTypically requires a high school diploma or associate degree; some roles prefer certification in clinical researchRequires a bachelor's degree, often in health sciences or related field; certification like CCRP is common
Work EnvironmentSupports data entry, management, and documentation in clinical trial settingsManages entire study processes, including patient recruitment, compliance, and coordination
Employer & IndustryHospitals, research institutions, pharmaceutical companiesResearch sites, hospitals, academic institutions

The Clinical Research Data Assistant primarily handles data-related tasks within clinical trials, while the Clinical Research Coordinator oversees the entire study process. Both roles are essential in clinical research but differ in responsibilities and required qualifications.

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

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

What are popular job titles related to Clinical Research Data Assistant jobs in Riverside, CA?

For Clinical Research Data Assistant jobs in Riverside, CA, the most frequently searched job titles are:

What job categories do people searching Clinical Research Data Assistant jobs in Riverside, CA look for?

The top searched job categories for Clinical Research Data Assistant jobs in Riverside, CA are:

What cities near Riverside, CA are hiring for Clinical Research Data Assistant jobs?

Cities near Riverside, CA with the most Clinical Research Data Assistant job openings:

Dietitian / Clinical Research Coordinator

Irvine Clinical Research

Riverside, CA

$30 - $40/hr

Full-time

Re-posted 9 days ago


Job description

Irvine Clinical Research is the largest independent clinical trial group on the West Coast. We're expanding our research in GLP-1 and incretins, testing the efficacy and safety of investigational anti-obesity medications. Can these drugs help participants manage their weight, reduce their risk of developing obesity-related complications, or even help with conditions such as depression?
 
As a Research Dietitian / Coordinator, you will play a crucial role in these clinical trials. In this hybrid role, you will be expected to counsel study participants on lifestyle measures while coordinating clinical trials. Your work may contribute to the advancement of truly life-changing treatments.
Job Duties
  • Conduct lifestyle counseling visits to improve nutrition and dietary quality, mental health/coping skills, and health behavior habits
  • Manage daily operations for assigned clinical trial projects
  • Perform study procedures in accordance with GCP and study protocols
  • Organize and maintain paper and electronic study data in a complete and correct manner
  • Cultivate enthusiastic and professional relationships with study participants and sponsors alike
  • Work closely with recruitment and prescreening teams to meet study enrollment goals
  • Conduct diagnostic, efficacy, and safety assessments as needed
Job Qualifications
  • Bachelor's or graduate degree from an accredited dietetics program
  • Valid Registered Dietitian (RD) or Registered Dietitian Nutritionist (RDN) Certification
  • Attention to detail and the ability to handle multiple tasks with precision
  • A command of professional spoken and written English
  • One (1) or more years of clinical research experience
Hours and Compensation
This is a partial full time (30 hours/week) employment position based in-person in Long Beach, Irvine, or Riverside on Mon-Thu 8:00a-4:00p.
 
The starting salary for this position is $30/hour. Higher salary is negotiable with candidates who have more experience with pharmaceutical clinical trials.
 
The company pays for 100% of health/dental/vision individual insurance costs for eligible full-time employees. Vacation (PTO) for this role will be earned at a rate of 11.25 days per year.