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Entry Level Clinical Data Analyst Jobs in Riverside, CA

IQVIA

Clinical Research Coordinator

Loma Linda, CA · On-site

$35 - $42/hr

About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and clinical ... Collect and accurately record clinical data in case report forms (CRFs). * Collaborate with ...

Little Scholars Services LLC

Be Seen First

Behavior Therapist

Eastvale, CA · On-site

$18 - $25/hr

Overall, it's a part-time, entry-level clinical role focused on meaningful behavior change, skill ... Collect session data and notes (we'll train you on everything) Support Families: Work ...

Little Scholars Services LLC

Be Seen First

Behavior Therapist

Eastvale, CA · On-site

$18 - $25/hr

Overall, it's a part-time, entry-level clinical role focused on meaningful behavior change, skill ... Collect session data and notes (we'll train you on everything) Support Families: Work ...

Pharmacy Careers

Pharmacovigilance Pharmacist

Fontana, CA · On-site +1

$59.25 - $71.25/hr

Analyze adverse event reports and clinical trial safety data. * Prepare regulatory submissions (e.g., MedWatch, PSURs). * Collaborate with medical affairs and clinical teams to address safety signals.

Pwc

AI & GenAI Data Scientist - Manager

Irvine, CA

$99K - $232K/yr

Industry/Sector Not Applicable Specialism Data, Analytics & AI Management Level Manager & Summary ... PwC does not intend to hire experienced or entry level job seekers who will need, now or in the ...

Pwc

AI & GenAI Data Scientist-Senior Associate

Irvine, CA · On-site

$77K - $202K/yr

Industry/Sector Not Applicable Specialism Data, Analytics & AI Management Level Senior Associate ... PwC does not intend to hire experienced or entry level job seekers who will need, now or in the ...

ABA Enhancement LLC

BCBA/Clinical Manager

Riverside, CA · On-site

$75K - $80K/yr

Additionally, this role involves ongoing data analysis and program adjustments to optimize therapeutic outcomes. Ultimately, the Clinical Supervisor ensures compliance with ethical standards and ...

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Entry Level Clinical Data Analyst information

See Riverside, CA salary details

$18

$37

$63

How much do entry level clinical data analyst jobs pay per hour?

As of Jun 14, 2026, the average hourly pay for entry level clinical 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 are some typical daily responsibilities for an Entry Level Clinical Data Analyst?

As an Entry Level Clinical Data Analyst, your daily responsibilities typically include reviewing and cleaning clinical trial data, performing data entry or validation tasks, generating standard reports, and assisting with database testing and documentation. You may work closely with senior data analysts, clinical research coordinators, and project managers to ensure data accuracy and compliance with regulatory standards. Collaboration and communication are key, as you’ll often participate in team meetings to discuss data queries or project updates. This hands-on experience helps build a strong foundation for future growth in the clinical data management field.

What does entry mean?

In the context of an Entry Level Clinical Data Analyst position, 'entry' indicates a role suitable for candidates with minimal professional experience, often requiring basic knowledge of data management, clinical research processes, and tools like Excel or SQL. It typically involves supervised tasks and offers opportunities for skill development and career growth within the healthcare or pharmaceutical industries.

What are the key skills and qualifications needed to thrive in the Entry Level Clinical Data Analyst position, and why are they important?

Entry Level Clinical Data Analysts need foundational knowledge in statistics, data management, and healthcare terminology, usually supported by a degree in a related field such as life sciences, health informatics, or mathematics. Familiarity with data analysis software like Microsoft Excel, SAS, or SQL, and exposure to clinical trial management systems or electronic data capture (EDC) platforms are beneficial. Strong attention to detail, problem-solving abilities, and effective communication skills help individuals excel in this role. These competencies are crucial for ensuring accurate and reliable data collection, analysis, and reporting that directly support clinical research outcomes.

What is the synonym for entry?

In the context of an Entry Level Clinical Data Analyst position, a synonym for 'entry' is 'beginner' or 'junior,' indicating a role suitable for those with limited experience. These roles often require foundational skills in data management, basic knowledge of clinical research, and familiarity with tools like Excel or SQL.

Is it entree or entry?

The correct term for the job level is 'entry' level, as in Entry Level Clinical Data Analyst. This designation indicates a position suitable for candidates with minimal professional experience, often requiring basic knowledge of data management tools like Excel or SQL. 'Entree' is a culinary term and not related to job levels.

Is it entry or entery?

The correct term for starting level positions, including entry level clinical data analyst roles, is 'entry,' not 'entery.' This term indicates a beginner or junior position that typically requires minimal experience and may involve on-the-job training or certifications. Proper spelling is important when applying or referencing job titles to ensure clarity and professionalism.

What is an Entry Level Clinical Data Analyst job?

An Entry Level Clinical Data Analyst is responsible for collecting, cleaning, and analyzing clinical data to support healthcare research and decision-making. They work with databases, statistical tools, and reporting software to ensure data accuracy and integrity. Their role often includes identifying trends, generating reports, and assisting in regulatory compliance. This position requires analytical skills, attention to detail, and knowledge of clinical terminology and data management systems. It is a great starting point for individuals interested in healthcare analytics and clinical research.

What are the most commonly searched types of Clinical Data Analyst jobs in Riverside, CA? The most popular types of Clinical Data Analyst jobs in Riverside, CA are:
What are popular job titles related to Entry Level Clinical Data Analyst jobs in Riverside, CA? For Entry Level Clinical Data Analyst jobs in Riverside, CA, the most frequently searched job titles are:
What job categories do people searching Entry Level Clinical Data Analyst jobs in Riverside, CA look for? The top searched job categories for Entry Level Clinical Data Analyst jobs in Riverside, CA are:
What cities near Riverside, CA are hiring for Entry Level Clinical Data Analyst jobs? Cities near Riverside, CA with the most Entry Level Clinical Data Analyst job openings:
Entry Level Clinical Data Analyst jobs near you
Infographic showing various Entry Level Clinical Data Analyst job openings in Riverside, CA as of June 2026, with employment types broken down into 1% As Needed, 85% Full Time, 2% Part Time, 1% Temporary, 10% Contract, and 1% Nights. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $78,897 per year, or $37.9 per hour.
Clinical Research Data Scientist (RWE)

Clinical Research Data Scientist (RWE)

Masimo

Irvine, CA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 15 days ago

Job description

Job Description
Job Summary:
Masimo is dedicated to developing innovative evidence solutions and critical insights through diverse data sources including Real World Data (RWD), trial data (collected internally and externally) and emerging innovative data sources, to support our clinical/scientific programs and regulatory submissions. The Clinical Research Data Scientist- Real World Evidence (RWE) and Outcomes Research will collaborate closely with strategic partners in Clinical Research , Engineering, Marketing, Medical Affairs and Payor Relations to develop and implement evidence and insights to improve patient outcomes and help meet unrealized marketing claims, and support regulatory activities.
Duties & Responsibilities:
Study Design and Statistical Planning
  • Contribute towards study protocols and study designs by developing and maintaining statistical analysis plans, simulation studies, and innovative methodologies tailored to multimodal datasets.
  • Apply rigorous statistical methodologies ensuring reproducibility, robustness, and regulatory readiness.

Evidence Generation
  • Implement real world evidence (RWE) generation strategies using conventional clinical study data and RWD to articulate value, address unmet needs, and support portfolio planning, commercialization, and patient access.

Data Science, Analytics and Management
  • Apply advanced statistical methods to large-scale datasets, including EHRs, claims, registries and longitudinal cohort studies.
  • Develop and execute data management plans across various relational databases, with proficiency in data cleaning, manipulation, and database management.
  • Collaborate with internal and external data management and statistical programming teams to generate research datasets and deliver insights.
  • Dive deep into data to uncover trends, identify key insights, and craft machine learning models to improve the accuracies, minimize resource usage and maximize the ease of use of existing and future Masimo products.
  • Improve data storage architectures and collection protocols

Strategic Business Partnership and Market Access
  • Translate analytical findings, develop compelling narratives, and generate visualizations that connect evidence generation to business objectives, enabling alignment across product development, payer engagement, and policy planning.
  • Collaborate cross-functionally with colleagues across Masimo to meet organizational objectives.
  • Work collaboratively with Payor Relations to support efforts to expand patient access to Masimo Technologies by generating statistical key evidence to support private and public payer coverage decisions

Clinical and Scientific Communication / Publications
  • Collaborate with physicians and clinical experts to develop high-quality clinical papers, abstracts, and presentations, resulting in publications in top-tier, peer-reviewed journals.
  • Communicate findings and methodologies clearly to scientific, clinical, and non-technical stakeholders.

Regulatory, Quality and Compliance
  • Ensure all projects comply with ethical standards, regulatory requirements, and internal quality guidelines.

Minimum & Preferred Qualifications and Experience:
Minimum Qualifications:
  • Minimum 3 years of experience in the medical device, pharma or healthcare industry, preferably in health economics, epidemiology, real-world evidence generation, outcomes research, or related functions.
  • Familiarity with and exposure to clinical development processes, research study designs and data analysis methods to include statistical analyses.

Preferred Qualifications:
  • Experience working with datasets from patient monitoring solutions and wearables (e.g., Blood pressure, Pulse Rate, ECG, Respiratory Rate, EEG, Alarms Data, EMR, hospital administrative metrics) and understanding of their clinical context is desired.
  • Demonstrated experience executing evidence generation strategies using RWD and managing multiple research projects concurrently (e.g., claims, EMR, administrative data, adaptive clinical trial designs).
  • Experience contributing to research activities across the study lifecycle, including developing research questions, assessing data feasibility, supporting study design, analysis, and interpretation.
  • Proficiency in applied statistics, statistical programming and database languages (SQL, R, Python, MATLAB, Pandas etc.)
  • Familiarity with AI frameworks such as Pytorch, Tensorflow, Keras, etc.), desired.
  • Experience working with real-world data (EHR, claims, registries, digital health) and familiarity with their opportunities and limitations.
  • Knowledge of endpoint validation frameworks and regulatory requirements (e.g., FDA/EMA).
  • Experience working with external partners and customers to support market access, portfolio planning, and commercialization initiatives using data and evidence.
  • Experience collaborating with hospitals, physicians, and professional organizations to help advance health economics and reimbursement activities in support of commercialization and sales/marketing objectives.
  • Outstanding organizational, verbal, and written communication skills, with the ability to create statistical visualizations in support of technical and business reports, internal presentations, and publication-ready manuscripts.

Education:
  • Ph.D. or M.S. degree in Bioinformatics, Computational Biology, Computer Science, Health Economics, Mathematics, Physics or similar quantitative discipline preferred.

Compensation: The anticipated range for this position is $100,000 - $140,000. Actual placement within the range is dependent on multiple factors, including but not limited to skills, education, and experience. This position also qualifies for up to 10% annual bonus based on Company, department, and individual performance.
  • Masimo offers benefits such as Medical, Dental, Vision, Life/AD&D, Disability Insurance, 401(k), Vacation, Sick, Holiday, Paid Maternity Leave, Flexible Spending Accounts, voluntary Accident, Critical Illness, Hospital, Long-Term Care, Employee Assistance Program, Pet Insurance, on-site Wellness Clinic, Fitness Center, Café. All benefits are subject to eligibility requirements.

Physical requirements/Work Environment
This position primarily works in an office environment. It requires frequent sitting, standing and walking. Daily use of a computer and other computing and digital devices is required. May stand for extended periods when facilitating meetings or walking in the facilities. Some travel is necessary, approximately 10%.
The physical demands of the position described herein are essential functions of the job and employees must be able to successfully perform these tasks for extended periods. Reasonable accommodations may be made for those individuals with real or perceived disabilities to perform the essential functions of the job described.
#LI-Onsite
About Us
For over thirty years, Masimo has been expanding the boundaries of noninvasive monitoring to improve patient outcomes and reduce the cost of care. Today, Masimo delivers a portfolio of hospital-trusted monitoring solutions to help increase patient safety, health, and wellness in the hospital and at home. When you join our team, you'll be part of a culture that's driven by passion, challenging the status quo, and making an impact in the lives of others.
This employer participates in the federal E-Verify program to confirm the identity and employment authorization of all newly hired employees. For further information about the E-Verify program, please click here: click here
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About Masimo

Sourced by ZipRecruiter

Industry

Medical equipment and supplies manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

Irvine, CA, US

Year founded

1989

Social media

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