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Senior Research Analyst Jobs in Riverside, CA (NOW HIRING)

Hyundai Glovis

Senior Analyst - Cost Assurance

Irvine, CA · On-site

$53/hr

Summary The Senior Analyst, Cost Assurance supports the end-to-end cost assurance cycle by ensuring ... Research, analyze, and resolve invoice discrepancies, payment exceptions, and AP/AR issues while ...

Direct Counsel

Senior Conflicts Analyst

Irvine, CA · On-site +1

$100K - $120K/yr

Excellent analytical, research, and communication skills, with the ability to deliver objective ... If you're a Senior Conflicts Analyst looking for an opportunity to take your expertise to a top ...

Akumincorp

Sr. Financial Analyst

Irvine, CA

$91K - $114K/yr

The Senior Financial Analyst provides analytical support in preparing regional financial budgets ... Provides research and analytical support for region specific initiatives. Provides comprehensive ...

Zymo Research

Research Intern Sample Prep

Tustin, CA · On-site

$20/hr

You will be mentored by a senior team member to support and effectively guide your contributions to ... Record and analyze results and regularly present findings and progress to the research team.

Akumin

Sr. Financial Analyst

Irvine, CA · On-site

$91K - $114K/yr

The Senior Financial Analyst provides analytical support in preparing regional financial budgets ... Provides research and analytical support for region specific initiatives. Provides comprehensive ...

Cornerstone Research

Analyst

Pomona, CA · On-site

$112K/yr

Many Analysts also choose to stay at Cornerstone Research and continue their careers with the firm - a number of our senior consultants, including Partners, started their careers as Analysts. In ...

Berkadia

Senior Financial Analyst

Irvine, CA · On-site

$91K - $114K/yr

Be Berkadia Berkadia is seeking a Senior Financial Analyst with 3-5 years of applicable experience ... Research, draft, and proof market intelligence for use in marketing collateral. Prepare and present ...

Jj

Senior Clinical Research Scientist

Irvine, CA · Hybrid

The Senior Clinical Research Scientist will join the Clinical Science & External Research (CSER ... Analyze and interpret clinical data; effectively communicate data using well-structured tables and ...

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Showing results 21-40

All JobsResearch Analyst JobsSenior Research Analyst JobsSenior Research Analyst Jobs in Riverside, CA

Senior Research Analyst information

See Riverside, CA salary details

$53.2K

$116.3K

$122.6K

How much do senior research analyst jobs pay per year?

As of Aug 11, 2026, the average yearly pay for senior research analyst in Riverside, CA is $116,267.00, according to ZipRecruiter salary data. Most workers in this role earn between $121,000.00 and $121,500.00 per year, depending on experience, location, and employer.

How much does a senior research analyst make in the US?

A senior research analyst in the US typically earns an average salary of around $70,000 to $90,000 per year, depending on experience, industry, and location. They often require strong analytical skills, proficiency with data tools, and relevant certifications to advance in their roles.

What does a senior research analyst do?

A senior research analyst works for a company in an analytical capacity, researching market information and technical data. In this career, your job duties are to gather information about the company, the markets, and other information from various sources, analyze the data, and write reports based on your findings. The qualifications needed for a career as a senior research analyst include a bachelor’s degree and experience relevant to your field. You also need several years of experience in a lower level analyst role, strong written and verbal communication skills, and computer proficiency.

What does a senior research analyst do?

A Senior Research Analyst is responsible for conducting advanced data analysis, interpreting complex information, and providing insights to support business decisions. They typically design research methodologies, collect and evaluate data from various sources, and present findings to stakeholders. Senior Research Analysts often mentor junior analysts, ensure data accuracy, and may specialize in specific industries like finance, marketing, or healthcare. Their work helps organizations identify trends, forecast outcomes, and develop effective strategies.

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

To thrive as a Senior Research Analyst, you need advanced analytical skills, expertise in research methodologies, and a relevant degree such as in economics, statistics, or business. Familiarity with data analysis tools like SPSS, SAS, R, or Tableau, as well as experience with database management and research software, is typically required. Strong communication, critical thinking, and problem-solving abilities distinguish top performers in this role. These skills are crucial for extracting actionable insights from complex data, informing strategic decisions, and effectively presenting findings to stakeholders.

What is the difference between Senior Research Analyst vs Research Analyst?

AspectSenior Research AnalystResearch Analyst
Required CredentialsBachelor's degree, often a master's; experience preferredBachelor's degree typically sufficient
Work EnvironmentMore complex projects, mentorship rolesData collection, analysis, reporting
Employer & Industry UsageFinancial, market research, consulting firmsSimilar industries, entry to mid-level roles
Common Search & ComparisonOften compared for career progressionBaseline role for research careers

The main difference between a Senior Research Analyst and a Research Analyst lies in experience, project complexity, and responsibilities. Senior Research Analysts typically handle more advanced projects, mentor junior staff, and require more experience or advanced degrees. Research Analysts focus on data collection and analysis at an entry or mid-level. Both roles are common in finance, market research, and consulting industries, with the senior position representing a step up in expertise and leadership.

How does a senior research analyst typically contribute to cross-functional projects within an organization?

Senior Research Analysts often play a crucial role in cross-functional projects by providing data-driven insights and market analysis to support strategic decision-making. They collaborate closely with teams such as marketing, product development, and finance, translating complex research findings into actionable recommendations tailored to each department's needs. This role frequently involves presenting results to stakeholders, aligning research objectives with business goals, and ensuring that projects are informed by the latest industry trends and reliable data sources.
More about Senior Research Analyst jobs
What are the most commonly searched types of Research Analyst jobs in Riverside, CA? The most popular types of Research Analyst jobs in Riverside, CA are:
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What cities near Riverside, CA are hiring for Senior Research Analyst jobs? Cities near Riverside, CA with the most Senior Research Analyst job openings:
Senior Research Analyst jobs near you
Infographic showing various Senior Research Analyst job openings in Riverside, CA as of August 2026, with employment types broken down into 1% Internship, 1% As Needed, 84% Full Time, 11% Part Time, and 3% Contract. Highlights an 86% Physical, 4% Hybrid, and 10% Remote job distribution, with an average salary of $116,267 per year, or $55.9 per hour.

Senior R&D Quality Officer, Product Development Quality Assurance

AbbVie

Irvine, CA • On-site

$109K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 5 days ago

AbbVie rating

8.6

Company rating: 8.6 out of 10

Based on 101 frontline employees who took The Breakroom Quiz

16th of 86 rated pharmaceutical

Job description

Company Description
About AbbVie
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.
Job Description
Purpose
This position is within the Product Development Quality Assurance (PDQA) organization and supports the timely review and disposition of batch documentation to help ensure uninterrupted clinical supply, advance the R&D pipeline, and maintain compliance with AbbVie standards and global GMP requirements. The role supports New Biological Entities (NBE), New Chemical Entities (NCE), and Advanced Therapy Medicinal Products (ATMP) across all phases of development, partnering with Third Party Manufacturers (TPM), AbbVie commercial manufacturing sites, and cross-functional teams to ensure drug substance and drug product for clinical use meet quality and regulatory requirements.
Job Description
The Senior R&D Quality Officer is responsible for GMP batch documentation review and clinical supply disposition for NBE, NCE, and ATMP development programs. This role applies deep QA expertise and GMP knowledge to ensure quality oversight of manufacturing activities at TPMs and AbbVie commercial sites in accordance with global GMP requirements and AbbVie quality standards. The role also provides strategic quality leadership, cross-functional influence, and support for development and mentoring of junior PDQA quality staff.
Key responsibilities include, but are not limited to:
  • Works effectively in a global environment, supporting the global Quality Assurance organization and cross-functional teams across multiple regions and time zones.
  • Review and approve batch manufacturing records (master and executed) and quality documentation for drug substance and drug product clinical supply batches at TPMs and AbbVie sites; make batch disposition and quality release decisions per SOPs, quality agreements, and GMP requirements; and apply risk-based quality assessments to support timely, defensible decisions and clinical supply continuity.
  • Assess the quality impact of manufacturing changes affecting drug substances or drug products, with a focus on NBE/NCE/ATMP clinical supply programs.
  • Author, review, and approve quality system documents, including SOPs and manufacturing instructions, to ensure accuracy and sustained GMP compliance.
  • Lead deviation and investigation activities for documentation errors, batch discrepancies, and process failures; author, review, and approve deviation/change control plans, exception documentation, and CAPA plans; drive thorough root cause analysis, timely corrective action, and sustained batch record right-first-time improvements.
  • Support the development of quality agreements with TPMs and internal manufacturing sites; lead TPM and supplier quality oversight activities, including escalation, and qualification strategy discussions.
  • Provide quality approvals in materials management and electronic quality systems, ensuring traceability, data integrity, and compliance across the clinical supply chain.
  • Partner cross-functionally with Clinical Drug Supply Management, Development Sciences, and Operations to identify and mitigate quality and manufacturing risks early in the batch lifecycle, protect batch availability, and ensure clinical supply continuity; lead project team efforts to drive timely, risk-based resolution strategies.
  • Generate, monitor, and report key PDQA quality metrics including batch documentation cycle times, aging documents, deviation trends, repeat deviations, CAPA effectiveness, and release blockers; present data-driven findings and improvement recommendations to PDQA management.
  • Support inspection readiness activities, including document retrieval, participation in mock audits, and coordination of QA-related responses; ensure the PDQA function maintains a perpetual state of inspection readiness.
  • Contribute to continuous improvement initiatives that strengthen GMP compliance, reduce review burden, and improve the overall reliability and quality oversight of clinical supply operations.
  • Provide mentoring and informal training to newer QA staff and cross-functional partners on batch documentation standards, GMP expectations, and quality system requirements; provide formal development support to junior PDQA colleagues.

Qualifications
  • Bachelor's degree required, preferably in Biology, Chemistry, Biochemistry, Pharmacy, or Chemical Engineering; advanced degree (M.S. or Ph.D.) may be considered in lieu of experience.
  • 4-6 years of progressive Quality Assurance experience in the pharmaceutical, biotechnology, or related life sciences industry; 8+ years preferred. Clinical supply, GMP manufacturing and Quality Assurance experience strongly preferred.
  • Working knowledge of global GMP requirements for drug substance and drug product manufacturing across biologics, small molecules, and ATMPs, including ICH Q7, ICH Q10, 21 CFR Parts 210/211, and relevant EU GMP Annexes.
  • Demonstrated experience reviewing and approving complex GMP batch records and associated quality documentation; familiarity with electronic batch record and quality management systems is a strong asset.
  • Proven ability to manage multiple competing priorities in a dynamic, fast-paced development environment, maintaining rigorous attention to detail and consistently meeting disposition timelines critical to clinical trial supply.
  • Experience with TPM quality oversight, including supplier qualification, quality agreements, and performance monitoring.
  • Strong communication and interpersonal skills, with the ability to articulate quality positions, influence cross-functional decisions, and partner effectively across levels.
  • Demonstrated problem-solving skills, with the ability to apply technical knowledge and sound quality judgment to independently resolve complex GMP issues, including time-sensitive situations impacting patient supply.

Additional Information
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
  • The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
  • We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
  • This job is eligible to participate in our long-term incentive programs.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company's sole and absolute discretion, consistent with applicable law.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
https://www.abbvie.com/join-us/reasonable-accommodations.html

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About AbbVie

Sourced by ZipRecruiter

AbbVie's mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas: immunology, oncology, neuroscience, eye care, virology, women's health, and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube, and LinkedIn.

Industry

Scientific research and development services

Company size

10,000+ Employees

Headquarters location

North Chicago, IL, US

Year founded

2013

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