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Clinical Research Data Analyst Jobs in Riverside, CA

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Clinical Research Data Analyst information

See Riverside, CA salary details

$18

$37

$63

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

As of Aug 10, 2026, the average hourly pay for clinical research data analyst in Riverside, CA is $37.93, according to ZipRecruiter salary data. Most workers in this role earn between $30.58 and $43.89 per hour, depending on experience, location, and employer.

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

AspectClinical Research Data AnalystClinical Research Coordinator
CredentialsBachelor's degree in health, science, or related field; proficiency in data analysis toolsBachelor's degree in health, science, or related field; clinical research certifications often preferred
Work EnvironmentData-focused roles in research settings, analyzing and managing dataOperational roles in clinical sites, managing study logistics and patient coordination
Employer & IndustryPharmaceutical companies, research institutions, CROsHospitals, clinics, research sites, pharmaceutical companies
Search & Comparison IntentUnderstanding data analysis roles in clinical researchManaging clinical trial operations and patient interactions

The Clinical Research Data Analyst primarily focuses on analyzing and managing research data, while the Clinical Research Coordinator handles study logistics and patient coordination. Both roles are essential in clinical trials but differ in responsibilities and daily tasks.

How to become a clinical research data analyst?

To become a clinical research data analyst, typically a bachelor's degree in a related field such as biology, statistics, or health sciences is required. Gaining experience with data management tools like SAS, R, or SQL, and understanding clinical trial processes are important. Some roles may also require certification in clinical research or data analysis to enhance job prospects.

What are the key skills and qualifications needed to thrive as a clinical research data analyst, and why are they important?

To thrive as a Clinical Research Data Analyst, a strong background in statistics, data management, and clinical research methodologies—often supported by a degree in a quantitative or health-related field—is essential. Familiarity with data analysis tools such as SAS, R, or Python, as well as experience with clinical trial management systems and regulatory standards, is typically required. Attention to detail, problem-solving, and effective communication are standout soft skills in this role. These skills ensure accurate data interpretation, regulatory compliance, and clear reporting of research findings critical to successful clinical studies.

What are some common challenges a clinical research data analyst faces when working with diverse clinical trial data?

Clinical Research Data Analysts often encounter challenges when standardizing and integrating data from multiple sources, such as different electronic health record systems or varying study protocols. Ensuring data accuracy, consistency, and compliance with regulatory standards can be complex, especially in multi-site or multinational trials. Additionally, analysts must frequently collaborate with clinical teams, statisticians, and IT professionals to resolve data discrepancies and implement robust data management solutions. Effective communication and adaptability are key to overcoming these challenges and ensuring high-quality research outcomes.

What does a clinical research data analyst do?

A clinical research data analyst is responsible for collecting, managing, and analyzing data from clinical trials to ensure accuracy and compliance. They use statistical tools and software to interpret data, prepare reports, and support decision-making in medical research projects.
What cities near Riverside, CA are hiring for Clinical Research Data Analyst jobs? Cities near Riverside, CA with the most Clinical Research Data Analyst job openings:
Infographic showing various Clinical Research Data Analyst job openings in Riverside, CA as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 15% Part Time, and 4% Contract. Highlights an 87% Physical, 3% Hybrid, and 10% Remote job distribution, with an average salary of $78,897 per year, or $37.9 per hour.

Clinical Research Coordinator

Flourish Research

Murrieta, CA • On-site

$31 - $38/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 28 days ago


Job description

Valkyrie Clinical Trials, a Flourish Research company, is looking for motivated, talented, creative individuals who want to learn and grow in their careers while contributing to research that changes lives! We offer an excellent comprehensive benefits package, a supportive and collaborative work environment, and endless growth opportunities.
We are actively hiring Clinical Research Coordinators at our Murrieta site location.
The Clinical Research Coordinator assists the Investigators in executing Phase I, II, III, and IV clinical research trials in accordance with Standard Operating Procedures (SOPs), FDA and GCP guidelines, and study protocols while providing an impeccable patient experience in every, single interaction.
Shift:
Monday-Friday, 8:30 AM - 5 PM (occasional weekends)
Location: 25405 Hancock Ave, Suite 110, Murrieta, CA 92562
Compensation: $31.00-$38.00/hr depending on experience
RESPONSIBILITIES

  • Execute protocol-specified patient visits and procedures, which may include, but not limited to, phlebotomy, IVs, injections, vital signs, ECG/EKG, etc.
  • Document assessments and study data per regs/GCP; maintain complete source; accurately complete CRFs/eCRFs.
  • Obtain informed consent per federal regs, GCP, and IRB requirements.
  • Ethically recruit qualified subjects to meet enrollment timelines.
  • Complete required/ongoing training; attend investigator meetings/courses; stay current with changing regulations and Flourish policies.
  • Schedule and conduct visits per protocol timelines.
  • Protect confidentiality per HIPAA and all confidentiality agreements.
  • Report AEs promptly; report SAEs to sponsor within 24 hours and notify PI/Sub-I/supervisor.
  • Account for and ensure availability of trial materials (study drug, labs, CRFs, supplies).
  • Maintain and document communication with Leads, Managers, PIs/Sub-Is, and study team per protocol and policy.
  • Perform duties safely, and in a time-/cost-effective manner compliant with Flourish policies.
  • Represent Flourish professionally in all interactions.
  • Additional duties as assigned by management.

Requirements

  • Bachelor's degree preferred, but not required
  • Must have oncology clinical research experience
  • Minimum of two years of clinical research experience
  • Clinical skills highly preferred: vital signs, EKG/ECG, phlebotomy, and injections
  • Familiar with e-source reporting via an electronic platform
  • A clear understanding of ICH, FDA, and GCP regulations
  • Impeccable organizational skills and attention to detail
  • Excellent communication and interpersonal skills to effectively interact with the Principal Investigator, research team, Study Sponsor/CROs, potential subjects, and referral sources
  • An ethical compass that compels the candidate to be honest, detail-oriented, and self-driven
  • High-level critical thinking skills
  • Working knowledge of medical terminology and lab collection/processing/storage procedures
  • Proficiency with computers and Microsoft Office Suite

Flourish Research offers an excellent comprehensive benefits package, a supportive and collaborative work environment, and endless growth opportunities. Apply today to learn more about how you can join us in our mission to save and improve the lives of others!

Benefits

Health, dental, and vision insurance plans, 401(k) with a 100% employer match on the first 4% of employee contributions, tuition reimbursement, parental leave, referral program, employee assistance program, life insurance, disability insurance, and 15 days of PTO + 8 paid holidays and 2 floating holidays.

Flourish Research is where clinical trials thrive.
Flourish Research is one of the industry’s most progressive and diversified clinical trial organizations, with strong capabilities across cardiology, metabolic disorders, renal, oncology, CNS, pulmonology, and vaccine research.
At Flourish Research, we strive toward excellence. In clinical trials and healthcare, excellence means everyone deserves the best care, regardless of their race, color, gender identity, religion, ethnicity, physical abilities, age, sexual orientation, or veteran status. We embrace employees, customers, and patients from these underrepresented groups to help make this vision a reality.
Flourish Research is driven by a diverse and inclusive community of passionate people who are committed to improving the quality of life of communities around the world. Flourish is committed to a safe work environment where all employees, customers, and patients are included, and treated with dignity and respect.
Flourish Research strives to build an organization that attracts and leverages diversity in our staff, which reflects the diversity of our local communities. We promote education, acceptance, and inclusion because there is beauty in diversity. The more diversity we have in our team, the more unique perspectives, and ideas we share, and the better prepared we are to serve our communities. WE SEE YOU. WE ARE YOU. WE EMBRACE YOU. WE CELEBRATE YOU!
Flourish Research is an equal employment opportunity employer. Employment decisions are based on merit and business needs, and not on race, color, sex, (including pregnancy and gender identity), citizenship status, national origin, ancestry, gender, sexual orientation, age, religion, creed, physical or mental disability, genetic information, marital status, veteran status, political affiliation, or any other factor protected by law. Flourish Research complies with the law regarding reasonable accommodation for handicapped and disabled employees.