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Clinical Research Data Assistant Jobs in Riverside, CA

Kelly Services

Clinical Research Specialist

Irvine, CA · Hybrid

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 ...

Jj

Clinical Research Leader

Irvine, CA · On-site +1

Is responsible for clinical data review to prepare data for statistical analyses and publications ... May assist with the development of Post-Market Clinical Follow-up (PMCF) Plans and PMCF Evaluation ...

Johnson & Johnson

Clinical Research Leader

Irvine, CA · On-site +1

Is responsible for clinical data review to prepare data for statistical analyses and publications ... May assist with the development of Post-Market Clinical Follow-up (PMCF) Plans and PMCF Evaluation ...

Johnson and Johnson

Clinical Research Leader

Irvine, CA · On-site +1

Is responsible for clinical data review to prepare data for statistical analyses and publications ... May assist with the development of Post-Market Clinical Follow-up (PMCF) Plans and PMCF Evaluation ...

Kelly Services

Clinical Research Specialist

Irvine, CA · On-site

Clinical Research Specialist DUTIES & RESPONSIBILITIES Under general direction and in accordance ... Assists in clinical data review to prepare data for statistical analyses and publications * May ...

Orion Group

Clinical Operations Support

Orange, CA · On-site

$19 - $23.50/hr

... data entry activities. * Maintain organized electronic and physical study records. * Assist the ... General knowledge of clinical research regulations and guidelines, including GCP, ICH, and ...

Jj

Clinical Research Leader, Neurovascular

Irvine, CA · On-site +1

Is responsible for clinical data review to prepare data for statistical analyses and publications ... May assist with the development of Post-Market Clinical Follow-up (PMCF) Plans and PMCF Evaluation ...

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Clinical Research Data Assistant information

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

As of Sep 5, 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 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 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 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 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:

Clinical Research Data Assistant jobs near you

Regulatory Research Assistant - (Clinical Research)

CenExel CIT

Riverside, CA

$20 - $22/hr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 3 days ago

New

Job description

About Us:

Each of CenExel’s research sites specialize in Phase I to Phase IV clinical trials. Our Centers of Excellence comprise some of the most well respected and long-standing research facilities in the country. Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology. Each of our Centers of Excellence has tremendous experience and expertise in complex early phase trials, and all our sites have in-patient capability. We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success.

Along with an exceptional work environment that promotes teamwork, positive leadership, and optimal work-life balance, CenExel Clinical Research also provides highly competitive compensation and a generous benefits package to full time employees after 30 days of employment including Health Insurance, Dental, Vision, LTD, STD, Life Ins, and 401k.

Hourly Rate: $20.00 - $22.00/hour (depending on education, experience, and skillset)

Schedule: Monday - Friday 08:00 AM - 04:30 PM

Job Summary:

Assist the Regulatory Specialists/Manager in maintaining clinical trial documents for submission to regulatory agencies in accordance to site SOPs, ICH, GCP, and FDA guidelines.
SOPs (Standard Operating Procedures)
ICH (International Council for Harmonization)
GCP (Good Clinical Practices)
FDA (Food and Drug Administration) 

Essential Responsibilities and Duties:

  • Complies with current protocols, site SOPs, GCPs, IRB (Institutional Review Board) and FDA guidelines.
  • Uploads regulatory documents with RealTime eDOCs System and files is paper binders, as necessary.
  • Prepares, obtains, organizes and maintains regulatory and training documents in various storage mediums.
  • Tracks submissions and ensure timely filing of documents.
  • Obtains CVs (Curriculum Vitae) of external Investigators and other contract personnel and their signatures for appropriate regulatory documents.
  • Forwards revised copies of protocols, informed consents, and other pertinent study documents to appropriate staff.
  • Assists in obtaining necessary signatures from investigators.
  • Works closely with study sponsor/CRO and key clinical trial personnel on relevant regulatory document issues.
  • Ensures Clinical Conductor regulatory information is current.
  • Participates in team meetings and complies with training requirements.
  • Assists sponsors/CRO’s as needed.
  • Supports and ensures strictest adherence to best practices, FDA Code of Federal Regulations, ICH (International Conference on Harmonization), GCP (Good Clinical Practices), CenExel standard operating procedures, site working Practices, protocol, and company guidelines and policies.
  • Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.

Education/Experience/Skills:

  • Must be able to effectively communicate verbally and in writing.
  • Minimum: High School graduate or equivalent.
  • Minimum of 1 year of related experience in clinical research 
  • Must be self-directed and able to work with minimal supervision.
  • Able to take a flexible approach to shifting priorities.
  • Motivated to work consistently in a fast-paced and rapidly changing environment.

 

Working Conditions

  1. Indoor, Office environment.
  2. Essential physical requirements include sitting, typing, standing, and walking.
  3. Lightly active position, occasional lifting of up to 20 pounds.
  4. Reporting to work, as scheduled, is essential.
  5. Ability to work overtime, weekends, and/or holidays as needed.
  6. Ability to travel as needed.
  7. Remote work arrangement depending on location.

CenExel Clinical Research is an Equal Opportunity Employer. All applicants will be considered for employment without regards to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or status.

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