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Research Associate Jobs in Riverside, CA (NOW HIRING)

Associate, Clinical Research Role Level: Individual Contributor (IC) Supervisor/Manager Title: Director, Clinical Affairs Job Location & Environment: Irvine, CA, Corporate Office Summary: The ...

Associate, Clinical Research Role Level: Individual Contributor (IC) Supervisor/Manager Title: Director, Clinical Affairs Job Location & Environment: Irvine, CA, Corporate Office Summary: The ...

A Master's degree or relevant certifications (e.g., Certified Medical Writer, Certified Research Associate) is a preferred. Experience: * At least 3-5 years of experience in clinical research or ...

A Master's degree or relevant certifications (e.g., Certified Medical Writer, Certified Research Associate) is a preferred. Experience: * At least 3-5 years of experience in clinical research or ...

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Research Associate information

See Riverside, CA salary details

$17

$33

$48

How much do research associate jobs pay per hour?

As of May 30, 2026, the average hourly pay for research associate in Riverside, CA is $33.95, according to ZipRecruiter salary data. Most workers in this role earn between $27.36 and $38.61 per hour, depending on experience, location, and employer.

What Does a Research Associate Do?

As a research associate, you conduct research and analysis as directed by a senior researcher or project manager. Researchers work in a number of fields, including medical science, the social sciences, natural sciences, finance, management, and academia. Your specific duties and responsibilities differ depending on the field in which you work, but some features of your work are similar across industries. You typically do primary and secondary source research, organize and process data, analyze said data, and report on your findings to lead researchers or clinicians.

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

To thrive as a Research Associate, you need a strong background in research methodology, data analysis, and subject-specific knowledge, typically supported by a relevant bachelor's or master's degree. Familiarity with statistical software (such as SPSS, R, or Python), laboratory equipment, and research databases is often essential. Attention to detail, critical thinking, and clear written and verbal communication skills set outstanding Research Associates apart. These skills ensure accurate data collection, effective collaboration, and the production of reliable, impactful research outcomes.

What are some typical challenges a Research Associate might face when managing multiple research projects simultaneously?

As a Research Associate, juggling multiple projects often requires strong organizational skills and the ability to prioritize tasks effectively. You might encounter challenges such as balancing deadlines, coordinating with various team members, and adapting to shifting project goals or data requirements. Effective communication and proactive time management are essential to ensure each project progresses smoothly and meets its milestones. Many teams use project management tools and regular check-ins to help mitigate these challenges and support collaboration.

What are Research Associates?

Research Associates are professionals who support research projects in academic, scientific, or business settings. They assist with designing studies, collecting and analyzing data, and preparing reports or publications. Research Associates often work under the supervision of principal investigators or senior researchers, contributing their expertise to advance the goals of the project. Their responsibilities can vary depending on the field, but typically involve both administrative and hands-on research tasks.

What is the difference between Research Associate vs Research Scientist?

AspectResearch AssociateResearch Scientist
Required CredentialsBachelor's or Master's degree in relevant fieldMaster's or PhD in relevant field
Work EnvironmentLaboratories, research institutions, universitiesLaboratories, research institutions, industry settings
Employer & Industry UsageAcademic, government, non-profitAcademic, industry, biotech, pharma
Common Search & ComparisonYesYes

The main difference between a Research Associate and a Research Scientist lies in their educational requirements and level of experience. Research Associates typically hold a bachelor's or master's degree and assist in research projects, while Research Scientists usually have a PhD and lead research efforts. Both roles work in similar environments like labs and research institutions, but Research Scientists often have more independence and responsibility.

What are the most commonly searched types of Research jobs in Riverside, CA? The most popular types of Research jobs in Riverside, CA are:
What are popular job titles related to Research Associate jobs in Riverside, CA? For Research Associate jobs in Riverside, CA, the most frequently searched job titles are:
What job categories do people searching Research Associate jobs in Riverside, CA look for? The top searched job categories for Research Associate jobs in Riverside, CA are:
What cities near Riverside, CA are hiring for Research Associate jobs? Cities near Riverside, CA with the most Research Associate job openings:
Infographic showing various Research Associate job openings in Riverside, CA as of May 2026, with employment types broken down into 82% Full Time, 7% Part Time, 2% Temporary, 7% Contract, and 2% Nights. Highlights an 94% In-person, 2% Hybrid, and 4% Remote job distribution, with an average salary of $70,614 per year, or $33.9 per hour.
Associate, Clinical Research

Associate, Clinical Research

JenaValve

Irvine, CA

Other

Posted 2 days ago


Job description

Job Title: Associate, Clinical Research
Role Level: Individual Contributor (IC)
Supervisor/Manager Title: Director, Clinical Affairs
Job Location & Environment: Irvine, CA, Corporate Office
Job Description Summary: The Clinical Research Associate will report to the Director, Clinical Affairs, and will play a key role in proactively supporting the conduct of pre-market and or post-market clinical studies and ensure compliance with all regulatory requirements. The ideal candidate will have a thorough knowledge of Good Clinical Practices (GCP) and applicable regulations.
Job Responsibilities:
  • Support site management and interact with site coordinators, investigators, and field monitors in collecting data and resolving queries to meet the protocol requirements in a timely manner.
  • Ensure quality data management activities - i.e., data review, query generation and resolution. Generate status reports to clinical staff and management.
  • Maintain Trial Master Files and trackers for clinical trials.
  • Manage trial-related regulatory documents and provide follow-up action listings to ensure that all clinical documentation required by regulations and JenaValve procedures is current.
  • Conduct periodic audits of internal files to ensure compliance per site Institutional Review Board (IRB) and/or Ethics Committee (EC) policy (i.e. IRB continuing review approval period and expiration dates).
  • Provide clinical operational support during preparation for and conduct of all clinical audits and inspections.
  • Contribute to the development and implementation of departmental policies, standards, and process improvement initiatives.
  • Partner with management to manage external vendors, including ongoing supplier qualification.
  • Assist field clinical monitors in preparation for site training and monitoring visits
  • Support monitoring of sites on an as-needed basis.
Required Education and Experience:
  • At least 1 year of experience in clinical trial research is required (preferred in medical devices).
  • Advanced degree in a biological science / pharmacy/ nursing desired.
Skills and Abilities Required for This Job:
  • Proficient in clinical trial management and electronic data capture systems to document and record information.
  • Excellent communication skills (written and verbal English) so as to be able to build effective relationships with trial center staff and colleagues.
  • Some knowledge of GCPs governing the conduct of clinical trials, Medical Device Directive 93/42/EEC, ISO14155 and ICH guidelines.
  • Very organized and able to pay close attention to detail.
  • Team player with a willingness to help where needed and work with diverse people.
Physical Requirements
  • Ability to travel up to 20% time.