ZipRecruiter

Log In

1

Statistics Validator Jobs in Riverside, CA (NOW HIRING)

Cryoport

Validation Engineer

Irvine, CA · On-site

POSITION SUMMARY: The Validation Engineer - Consulting Services will support the Consulting ... Analytical thinker with proficient skills in math, statistics, and data analysis applications ...

Cryoport, Inc.

Validation Engineer

Irvine, CA · On-site

... math, statistics, and data analysis applications • Strong organizational skills to manage ... Process Validation using DQ, IQ, OQ, and PQ. • Knowledge of cGMP requirements, FDA and ICH ...

Cryoport

PD Validation Engineer

Irvine, CA · On-site

... with statistical data analysis and reporting (e.g., pivot tables, charts) PREFERRED SKILLS ... validation activities (logistics, pharmaceuticals, medical devices, etc.) Familiarity with ...

Cryoport, Inc.

PD Validation Engineer

Irvine, CA · On-site

... statistical data analysis and reporting (e.g., pivot tables, charts) PREFERRED SKILLS • ... validation activities (logistics, pharmaceuticals, medical devices, etc.) • Familiarity with ...

CYNET SYSTEMS

Senior Supplier Quality Engineer

Irvine, CA · On-site

$44 - $49/hr

Experience and/or proficient knowledge of Design Controls and test method development/validations. * Experience with statistical techniques and tools such as Gage R&R, Statistical Process Control, or ...

AbbVie

Associate Director, RWE Analytics

Irvine, CA · On-site

$141K/yr

... validation checks, organization, protection and security, documentation, and statistical methods. • Monitor scientific, regulatory and reimbursement / access trends, events and policies for their ...

next page

Showing results 1-20

All JobsStatistics Validator JobsStatistics Validator Jobs in Riverside, CA

Statistics Validator information

See Riverside, CA salary details

$42.3K

$87.3K

$122.1K

How much do statistics validator jobs pay per year?

As of Jun 16, 2026, the average yearly pay for statistics validator in Riverside, CA is $87,276.00, according to ZipRecruiter salary data. Most workers in this role earn between $59,500.00 and $121,000.00 per year, depending on experience, location, and employer.

What are Statistics Validators?

Statistics Validators are professionals who verify the accuracy, integrity, and reliability of statistical data and analyses. They review datasets, methodologies, and statistical outputs to ensure that findings are valid and meet relevant standards. Their work is crucial in research, government, and industry settings, where credible data is essential for decision making. By checking for errors, inconsistencies, and biases, Statistics Validators help maintain the quality and trustworthiness of statistical information.

What are the primary challenges a Statistics Validator faces when ensuring data integrity within a project?

Statistics Validators often encounter challenges related to data quality, such as incomplete datasets, inconsistent formats, or errors introduced during data collection and entry. They must meticulously review data sources, cross-check results, and ensure that statistical methodologies are correctly applied. Collaboration with data analysts, researchers, and IT teams is essential to resolve discrepancies and maintain high data standards. Staying up-to-date with industry best practices and regulatory requirements also plays a crucial role in overcoming these challenges.

What is the difference between Statistics Validator vs Data Analyst?

AspectStatistics Validator
Required CredentialsTypically a degree in statistics, mathematics, or related field; certifications like CAP or ASA are common
Work EnvironmentPrimarily office-based, working with data validation processes, quality assurance, and compliance
Employer & IndustryFinancial institutions, research organizations, government agencies, and data-driven companies
Comparison with Data Analyst

The main difference between a Statistics Validator and a Data Analyst lies in their focus. A Statistics Validator specializes in verifying the accuracy and integrity of statistical data, ensuring compliance with standards. In contrast, a Data Analyst interprets data to generate insights and support decision-making. While both roles require strong statistical knowledge, the validator emphasizes quality assurance, whereas the analyst emphasizes data interpretation and reporting.

What are the key skills and qualifications needed to thrive as a Statistics Validator, and why are they important?

To thrive as a Statistics Validator, you need a strong background in statistics, data analysis, and quality assurance, often supported by a degree in statistics, mathematics, or a related field. Familiarity with statistical software such as R, SAS, or SPSS, as well as proficiency in data validation frameworks and reporting tools, is typically required. Attention to detail, critical thinking, and strong communication skills help ensure the accuracy and clarity of validated data. These skills and qualities are crucial for maintaining data integrity, supporting decision-making, and upholding the credibility of statistical results.
What are popular job titles related to Statistics Validator jobs in Riverside, CA? For Statistics Validator jobs in Riverside, CA, the most frequently searched job titles are:
What cities near Riverside, CA are hiring for Statistics Validator jobs? Cities near Riverside, CA with the most Statistics Validator job openings:
Statistics Validator jobs near you
Infographic showing various Statistics Validator job openings in Riverside, CA as of June 2026, with employment types broken down into 63% Full Time, 28% Part Time, and 9% Nights. Highlights an 100% In-person job distribution, with an average salary of $87,276 per year, or $42 per hour.
Director Statistical Programming

Director Statistical Programming

Edwards Lifesciences Corporation

Irvine, CA • On-site

$182K - $257K/yr

Full-time

Posted 6 days ago

Edwards Lifesciences rating

8.3

Company rating: 8.3 out of 10

Based on 30 frontline employees who took The Breakroom Quiz

66th of 518 rated manufacturers

Job description

Imagine how your ideas and expertise can change a patient's life. We generate extensive clinical evidence to demonstrate the effectiveness and safety of our innovations and how our products transform patients' lives. As part of our Clinical Affairs team, you'll hone your scientific curiosity and passion for evaluating data to increase access to pioneering technologies for patients in need. In close partnership with principal investigators, dedicated medical professionals, patient advocacy groups, and regulatory authorities, you will drive the evidence needed to optimize patient outcomes.

Patients with mitral and tricuspid heart valve disease often have complex conditions with limited treatment options. Our Transcatheter Mitral and Tricuspid Therapies (TMTT) business unit is boldly pursuing an innovative portfolio of technologies to address a patient's unmet clinical needs. It's our driving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey.

How you'll make an impact:

  • As the Director of Statistical Programming, you will lead teams of programmers to develop, test, validate, document, maintain and execute programs in SAS to support statistical deliverables within agreed timelines. He/she will mentor and develop programmers and allocate statistical programming resources under the provided project priorities and timeline.

  • Facilitate talent management activities to include hiring, training, staff development and succession planning. Mentor and develop team of programmers by providing regular coaching and guidance. Manage people resource allocation of statistical programming.

  • Prepare, document, and review programming codes and output for own project and/or as needed to ensure the quality of programming output.

  • Review ADS Specs and output for own project and/or other projects

  • Ensure analysis data and programming code meet regulatory and company standards and are consistently structured to permit efficient programming, reporting, and review

  • Participate in the development of procedures and standards and adherence to existing procedures

  • Prepare analysis datasets

  • Develop program specification and design documents

What you'll need (Required):

  • Master's Degree in Computer Science or Statistics or other related fields

  • 11 Year experience Solid SAS programming experience on clinical data in the pharmaceutical and/or medical device industry.

  • 3 years' experience Managing statistical programmers

What else we look for (Preferred):

  • Proven successful project management leadership skills

  • Proven expertise in SAS and Windows operating systems required; experience using other software packages (e.g., R, S-Plus)

  • Proven expertise in MS Office Suite including Word, PowerPoint, Access, and Excel

  • Excellent written and verbal communication skills and interpersonal relationship skills including negotiating and relationship management skills with ability to drive achievement of objectives

  • Keeps abreast of new developments in statistics and regulatory guidance

  • Expert understanding of clinical trial and statistical programming procedures while addressing issues with impact beyond own team based on knowledge of related disciplines

  • Demonstrated track record in people management

  • Expert understanding and knowledge relevant to statistical programming

  • Expert understanding and knowledge of regulatory guidelines (e.g., GCP, ICH, FDA, ISO) relevant to in Pharmaceutical/Medical Device research setting

  • Excellent problem-solving, organizational, analytical and critical thinking skills

  • Demonstrated ability to manage assigned team and provide coaching and feedback, including responsibility for all employee actions including hire/fire authority and partnering with HR on all aspects of employee relations

  • Experience in facilitating change, including collaboration with management and executive stakeholder

  • Strict attention to detail

  • Ability to interact professionally with all organizational levels

  • Ability to manage competing priorities in a fast paced environment

  • Must be able to work in a team environment, including participating and presenting at meetings, including with external representatives

  • Frequently interacts with customers, and/or functional peer group managers, normally involving matters between cross-functional teams and the company; often leads a cooperative effort among members of a project team

  • Participate and present at meetings with internal and external representatives

Aligning our overall business objectives with performance, we offer competitive salaries, performance-based incentives, and a wide variety of benefits programs to address the diverse individual needs of our employees and their families.
The base pay range for this position is $182,000 to $257,000 (highly experienced).
The pay for the successful candidate will depend on various factors (e.g., geographic location, qualifications, education, prior experience). Applications will be accepted while this position is posted on our Careers website.

Edwards is an Equal Opportunity/Affirmative Action employer including protected Veterans and individuals with disabilities.

COVID Vaccination Requirement

Edwards is committed to protecting our vulnerable patients and the healthcare providers who are treating them. As such, all patient-facing and in-hospital positions require COVID-19 vaccination. If hired into a covered role, as a condition of employment, you will be required to submit proof that you have been vaccinated for COVID-19, unless you request and are granted a medical or religious accommodation for exemption from the vaccination requirement. This vaccination requirement does not apply in locations where it is prohibited by law to impose vaccination.

What Edwards Lifesciences employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

Edwards Lifesciences logo

About Edwards Lifesciences

Sourced by ZipRecruiter

Edwards Lifesciences is the global leader in patient-focused medical innovations for structural heart disease, as well as critical care and surgical monitoring. Driven by a passion to help patients, the company collaborates with the world's leading clinicians and researchers to address unmet healthcare needs, working to improve patient outcomes and enhance lives. Headquartered in Irvine, California, Edwards Lifesciences has extensive operations in North America, Europe, Japan, Latin America and Asia and currently employs over 15,000 individuals worldwide. For us, helping patients is not a slogan - it's our life's work. From developing devices that replace or repair a diseased heart valve to creating new technologies that monitor vital signs in the critical care setting, we focus on helping patients regain and improve the quality of their life.

Industry

Medical equipment and supplies manufacturing

Company size

10,000+ Employees

Headquarters location

Irvine, CA, US

Year founded

1958

View All Edwards Lifesciences Jobs

Apply