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Clinical Research Data Coordinator information

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$16

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

As of Sep 5, 2026, the average hourly pay for clinical research data coordinator in Riverside, CA is $29.93, according to ZipRecruiter salary data. Most workers in this role earn between $24.33 and $32.36 per hour, depending on experience, location, and employer.

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

To thrive as a Clinical Research Data Coordinator, you need a background in life sciences or health-related fields, strong attention to detail, and experience with data management in clinical research. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and knowledge of regulatory standards such as GCP or HIPAA is typically required. Strong organizational skills, effective communication, and the ability to work collaboratively make someone stand out in this role. These skills and qualities ensure accurate data collection, regulatory compliance, and efficient coordination of clinical research activities.

What are some typical challenges clinical research data coordinators face when managing study data, and how can they be addressed?

Clinical Research Data Coordinators often encounter challenges such as maintaining data accuracy, ensuring timely data entry, and managing large volumes of information from multiple sources. These challenges can be addressed by implementing rigorous quality control procedures, using electronic data capture systems, and maintaining clear communication with clinical teams. Developing strong organizational skills and staying updated on regulatory requirements are also essential for successfully managing these complexities.

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

AspectClinical Research Data CoordinatorClinical Research Associate
CredentialsTypically requires a bachelor's degree in health, life sciences, or related field; certifications like CCRP are a plusOften requires a bachelor's degree; certifications like CCRP or RAC are common
Work EnvironmentPrimarily works in data management, database entry, and ensuring data accuracy within clinical trial sites or officesWorks on-site or remotely overseeing trial conduct, monitoring sites, and ensuring protocol compliance
Employer & Industry UsageUsed by pharmaceutical companies, CROs, and research institutions focusing on data collection and managementUsed by sponsors, CROs, and research sites overseeing trial progress and compliance

While both roles support clinical trials, the Clinical Research Data Coordinator focuses on data entry and management, ensuring data quality. The Clinical Research Associate oversees trial conduct, site monitoring, and compliance. Both roles require similar educational backgrounds and certifications, but their daily responsibilities and work environments differ.

Are clinical research data coordinators in high demand?

Clinical research data coordinators are in high demand due to the growth of clinical trials and the need for accurate data management in healthcare research. The role often requires familiarity with electronic data capture systems and adherence to regulatory standards, making skilled coordinators valuable in the industry.

What does a clinical research data coordinator do?

A clinical research data coordinator manages and maintains data collected during clinical trials, ensuring accuracy, completeness, and compliance with regulatory standards. They often use data management tools like electronic data capture systems and collaborate with research teams to support study integrity and reporting.

What skills do you need to be a clinical research data coordinator?

A clinical research data coordinator needs strong attention to detail, proficiency in data management software such as electronic data capture (EDC) systems, and knowledge of clinical trial protocols and regulatory requirements. Good organizational skills, communication abilities, and the ability to work under deadlines are also essential. Familiarity with data privacy standards like HIPAA is important for maintaining confidentiality.

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 Coordinator jobs in Riverside, CA?

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

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

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

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

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

Clinical Research Data Coordinator jobs near you
Infographic showing various Clinical Research Data Coordinator job openings in Riverside, CA as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 13% Part Time, and 3% Contract. Highlights an 88% Physical, 3% Hybrid, and 9% Remote job distribution, with an average salary of $62,248 per year, or $29.9 per hour.

Clinical Research Site Manager

Headlands Research

Riverside, CA • On-site

Full-time

PTO

Re-posted 2 days ago

Job description

The Role

The Site Manager performs clinical research activities as a Clinical Research Coordinator while also serving as Manager of the site operations. The Site Manager owns meeting or exceeding financial targets, KPIs, and patient enrollment, as well as champions screening, patient retention, and partnering with other Headlands centralized departments or sites.

Position Type:  Full-time

Location:  Onsite in Riverside, CA

Responsibilities:

  • Strategic and Operational Management
    • Evaluates overall performance of the Site and recommends and implements processes and plans for improvement.
    • Responsible for maintaining a site calendar to ensure adequate enrollment for studies and coordination of employee PTO.
  • Staff Development and Management
    • Fosters a culture of excellence, teamwork, and innovation among site staff
    • Hires, trains, and mentors site staff, including Clinical Research Coordinators, Research Assistants, Administrative Assistants, Registered Nurses, support personnel, etc.
    • Partners with Human Resources and Management when hiring new employees for the site by reviewing candidate credentials, conducting interviews, and giving input about potential new hires
    • Supervises performance of other Clinical Research Coordinators, Research Assistants, and support staff at the Site
  • Quality Assurance & Compliance
    • Maintains up-to-date knowledge of all relevant regulatory guidelines and requirements
    • Ensures the site's compliance with FDA, ICH, and local regulatory agency regulations
  • Clinical Research Coordination
    • In addition to assuming management responsibilities as a Site Manager, this individual performs the duties of a Clinical Research Coordinator
    • Protects the rights, safety, and welfare of human subjects, follows Good Clinical Practice, and works cooperatively with others
    • Monitors study activities to ensure compliance with study protocols, with site policies, and with applicable federal, state, and local regulations
    • Oversee the planning, initiation, and execution of clinical trials at the site
    • Maintains required records of study activity including case report forms, drug dispensation records, and regulatory forms
    • Manages and optimizes patient recruitment and retention efforts
    • Assesses eligibility of potential subjects through methods such as screening interviews, reviews of medical records, and discussions with physicians and other healthcare professionals
    • Addresses any patient concerns or issues promptly and professionally
  • Documentation and Reporting
    • Documents findings and events in the CTMS platform and in other binders and platforms as directed
    • Reviews proposed study protocols to evaluate factors such as sample collection processes, data management plans, and potential subject risks
  • Performs other duties as assigned, including duties routinely performed by the Company's Research Assistants

 

Requirements:

  • 5+ years of experience as a delegated Clinical Research Coordinator on multiple phase 2-4 clinical research trials, simultaneously
  • Proficiency in FDA regulations governing clinical trials
  • Strong supervisory skills to lead research staff effectively
  • Ability to collect and manage research data accurately
  • Familiarity with documentation review processes in clinical research
  • Knowledge of medical terminology relevant to clinical trials management
  • IATA (dangerous goods handling)
  • GCP (Good Clinical Practice)
  • Strong communication skills with all members of the team.

Preferred Qualifications:

  • Bachelor's degree
  • Capability to perform phlebotomy procedures
  • CCRC or CCRP certified

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