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Clinical Data Associate Jobs in Riverside, CA (NOW HIRING)

CQI Specialist

San Bernardino, CA · On-site

$37.50 - $50/hr

Analyze operational and clinical data to support evidence-based decision making. * Track corrective ... Associate degree required; Bachelor's degree preferred in EMS, Healthcare Administration, Nursing ...

CQI Specialist

San Bernardino, CA · On-site

$61K - $75K/yr

Analyze operational and clinical data to support evidence-based decision making. * Track corrective ... Associate degree required; Bachelor's degree preferred in EMS, Healthcare Administration, Nursing ...

Clinical Operations Support

Orange, CA · On-site

$19 - $23.50/hr

Support accurate and timely data entry activities. * Maintain organized electronic and physical ... Bachelor's degree preferred/required; an Associate's degree may be considered with relevant ...

Showing results 41-60

Clinical Data Associate information

See Riverside, CA salary details

$14

$40

$90

How much do clinical data associate jobs pay per hour?

As of Sep 13, 2026, the average hourly pay for clinical data associate in Riverside, CA is $40.64, according to ZipRecruiter salary data. Most workers in this role earn between $30.58 and $40.62 per hour, depending on experience, location, and employer.

What does a clinical data associate do?

A Clinical Data Associate is responsible for collecting, validating, and managing clinical trial data to ensure its accuracy, completeness, and compliance with regulatory standards. They work closely with clinical research teams to monitor data quality, resolve discrepancies, and prepare data for analysis. Their work is essential in supporting drug development and regulatory submissions by ensuring reliable and high-quality clinical data.

What does a clinical data associate do?

A clinical data associate is responsible for tracking data and results in a research study. As a clinical data associate, your job duties are to collect data, perform data management, and input data into any software used by your team. You work on a research team, so you must be able to work collaboratively and have excellent organizational skills. While you spend most of your time in an office, you may be required to work in the field to record data. The only universal qualifications needed for this career are a background in health care or medical science research and experience with data management software like Oracle Clinical, Microsoft Excel, and SPSS.

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

To thrive as a Clinical Data Associate, you need a solid understanding of clinical research, data management principles, and attention to detail, often supported by a degree in life sciences or a related field. Familiarity with clinical data management systems (CDMS), electronic data capture (EDC) tools, and knowledge of regulatory guidelines like GCP or CDISC is typically required. Strong organizational skills, analytical thinking, and clear communication set outstanding candidates apart in this role. These skills ensure the accuracy, integrity, and compliance of clinical trial data, which are crucial for successful research outcomes and regulatory approval.

What are some common challenges faced by clinical data associates when ensuring data quality during clinical trials?

Clinical Data Associates often encounter challenges such as identifying and resolving discrepancies in large datasets, maintaining strict compliance with regulatory standards, and coordinating timely data entry from multiple sites. They must work closely with clinical research teams and data managers to clarify ambiguous data and implement data cleaning procedures. Staying organized and detail-oriented is essential to ensure data accuracy and the successful progression of clinical trials.

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

AspectClinical Data AssociateClinical Research Coordinator
Primary RoleManage and ensure accuracy of clinical trial dataOversee trial operations, patient recruitment, and site management
CredentialsBachelor's in life sciences or related field; familiarity with data managementBachelor's in health sciences or related field; clinical trial experience
Work EnvironmentData management teams, clinical trial databasesClinical sites, hospitals, research facilities
Industry UsagePharmaceutical companies, CROs, biotech firmsHospitals, research institutions, clinical trial sites

While both roles support clinical trials, a Clinical Data Associate primarily focuses on managing and validating trial data, ensuring accuracy and compliance. In contrast, a Clinical Research Coordinator handles the overall trial operations, including patient recruitment and site coordination. Both roles require relevant certifications and work within the clinical research industry, but their daily responsibilities differ significantly.

What are the most commonly searched types of Clinical Data jobs in Riverside, CA?

The most popular types of Clinical Data jobs in Riverside, CA are:

What are popular job titles related to Clinical Data Associate jobs in Riverside, CA?

For Clinical Data Associate jobs in Riverside, CA, the most frequently searched job titles are:

What job categories do people searching Clinical Data Associate jobs in Riverside, CA look for?

The top searched job categories for Clinical Data Associate jobs in Riverside, CA are:

What cities near Riverside, CA are hiring for Clinical Data Associate jobs?

Cities near Riverside, CA with the most Clinical Data Associate job openings:

Infographic showing various Clinical Data Associate job openings in Riverside, CA as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 15% Part Time, and 3% Contract. Highlights an 84% Physical, 4% Hybrid, and 12% Remote job distribution, with an average salary of $84,526 per year, or $40.6 per hour.

Associate Scientific Writer - Medical Devices

Rancho Santa Margarita, CA • On-site

Applied Medical
Medical Equipment and Supplies Manufacturing • 1 - 5K employees

$70K - $80K/yr

Full-time

Medical, Life, Retirement, PTO

Re-posted 12 days ago


Key responsibilities

  • Develop and complete scientific protocols and reports, including Clinical Evaluations and Post Market Clinical Feedback, to support product registrations for medical devices.

  • Review post-market data such as complaints and feedback, and incorporate relevant data and analysis into reports.

  • Evaluate scientific literature and research findings to inform report writing and ensure compliance with medical writing standards.


Applied Medical rating

7.3

Company rating: 7.3 out of 10

Based on 24 frontline employees who took The Breakroom Quiz


Job description

Applied Medical is a new generation medical device company with a proven business model and commitment to innovation fueled by rapid business growth and expansion. Our company has been developing and manufacturing advanced surgical technologies for over 35 years and has earned a strong reputation for excellence in the healthcare field.  Our unique business model, combined with our dedication to delivering the highest quality products, enables team members to contribute in a larger capacity than is possible in typical positions.


Position Description

Collaboration is a fundamental part of our organization's culture and is essential to our continued success. As such, the successful candidate for this position is expected to work fully on-site, enabling them to engage fully with colleagues and contribute to cross-functional initiatives. Therefore, the ability to work collaboratively and contribute to a positive and supportive team environment is a key requirement for this role. 

As an Associate Clinical Writer, you will work within the Clinical Affairs team. The Associate Clinical Writer’s primary responsibilities are developing and completing scientific protocols and reports, including, but not limited to, Clinical Evaluations and Post Market Clinical Feedback as part of design validations for medical devices to support product registrations internationally. You will conduct reviews of post-market data, such as complaints and feedback, to incorporate relevant data and analysis into reports.

Key Responsibilities:

  • Critical Thinking: You will need to be able to critically evaluate scientific literature and research findings and apply this knowledge to your work. This involves asking questions, identifying gaps in the research, and synthesizing information from multiple sources. 
  • Writing Skills: You will be responsible for conducting thorough literature searches to identify relevant studies, systematic reviews, and meta-analyses that inform your writing. You will also be responsible for creating and maintaining job aids and work instructions for the preparation and maintenance of compliant medical writing deliverables.
  • Communication: You will be responsible to manage timelines and communicate with team members to maintain awareness of expectations, milestones, and deliverables. You will also be expected to collaborate with cross-functional teams to develop new and insightful analytics to collect and analyze clinical data.

Position Requirements

This position requires the following skills and attributes:

  • Bachelor’s or Advanced degree in a scientific field (MS, Ph.D., MD, or Pharm. D.)
  • Experience in conducting focused literature searches on PubMed, Embase or other similar literature databases
  • Data mining and analysis
  • Ability to formulate reports and present findings
  • Effective written and oral communication skills
  • Ability to collaborate in a team environment
  • Project management and organizational skills
  • Strong familiarity with Microsoft Office

Preferred

The following skills and attributes are preferred:

  • 1-2 years of experience in the medical device/pharmaceutical field or 1+ years of research with professor
  • Ability to understand and interpret results of clinical studies, with a strong understanding of statistics
  • Experience performing statistical analysis with statistical programs
  • Ability to prioritize and manage multiple projects
  • Data analytic publication experience or literature author publication experience

***Please note that this role is internally titled 'Associate Clinical Writer'. Externally, we refer to it as 'Associate Scientific Writer - Medical Devices' to better reflect the role's responsibilities.


Benefits
  • Competitive compensation range: $70000 - $80000 / year (California). 
  • Comprehensive benefits package. 
  • Training and mentorship opportunities. 
  • On-campus wellness activities. 
  • Education reimbursement program. 
  • 401(k) program with discretionary employer match. 
  • Generous vacation accrual and paid holiday schedule. 

Please note that the compensation range may be adjusted in the future, and bonus and incentive compensation plans may apply. 

Our total reward package reflects our commitment to employee growth and well-being, as we invest in your development and offer a range of benefits designed to enhance your career and life. 

All compensation and benefits are subject to plan documents and written agreements. 

Equal Opportunity Employer

Applied Medical is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, color, disability (mental and physical), exercising the right to family care and medical leave, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, political affiliation, race, religious creed, sex (including pregnancy, childbirth, breastfeeding and related medical conditions), or sexual orientation, or any other status protected by federal, state or local laws in the locations where Applied Medical operates.

Qualifications:

This position requires the following skills and attributes:

  • Bachelor’s or Advanced degree in a scientific field (MS, Ph.D., MD, or Pharm. D.)
  • Experience in conducting focused literature searches on PubMed, Embase or other similar literature databases
  • Data mining and analysis
  • Ability to formulate reports and present findings
  • Effective written and oral communication skills
  • Ability to collaborate in a team environment
  • Project management and organizational skills
  • Strong familiarity with Microsoft Office
Education:UNAVAILABLEEmployment Type: FULL_TIME

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