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

Clinical Research Leader

Irvine, CA · On-site

$109 - $174.80/hr

  • PTO

Be responsible for clinical data review to prepare data for statistical analyses and publications ... May act as Clinical Safety Coordinator: coordinate all safety-related activities of clinical trials ...

Lead publications for clinical study data through coordination with investigator authors, writes appropriate sections, and reviews/revises abstracts and manuscripts. Serve as an active member of ...

The Clinical Evidence organization supports R&D, designs and analyzes clinical trials (from FIM to ... data through coordination with investigator authors, writes appropriate sections, and reviews ...

Responsibilities include patient recruitment, informed consent, trial coordination, data management, and regulatory compliance. The position requires in-depth knowledge of clinical trial regulations ...

Responsibilities include patient recruitment, informed consent, trial coordination, data management, and regulatory compliance. The position requires in-depth knowledge of clinical trial regulations ...

Regional Clinical Director

Orange, CA

$96K - $130K/yr

... deliver coordinated longitudinal outpatient care for this population. None of it has been built ... Translate KPI data into clear priorities for site teams; run regular clinical leadership check-ins ...

Spec 3, Clinical Research

Irvine, CA · On-site

  • Medical

  • Life

  • Retirement

The Specialist collaborates with cross-functional teams to resolve documentation and data issues ... Support clinical trial start-up activities, including site readiness tracking, coordination of Site ...

Clinical Research Associate

Irvine, CA · Remote

$120K - $135K/yr

The Clinical Research Associate (CRA) will support Clinical Operations in planning, coordinating ... Perform remote monitoring activities such as source data verification (SDV) and data entry checks ...

Showing results 21-40

Clinical Data Coordinator information

See Riverside, CA salary details

$16

$30

$59

How much do clinical data coordinator jobs pay per hour?

As of Aug 19, 2026, the average hourly pay for clinical data coordinator in Riverside, CA is $30.93, according to ZipRecruiter salary data. Most workers in this role earn between $23.85 and $35.38 per hour, depending on experience, location, and employer.

What does a clinical data coordinator do?

A Clinical Data Coordinator is responsible for collecting, managing, and ensuring the quality of data generated from clinical trials and medical research studies. They work closely with clinical research teams to input, verify, and monitor data accuracy, integrity, and compliance with regulatory standards. Their work is vital for the successful analysis of clinical trial outcomes and for supporting the development of new medical treatments.

What does a clinical data coordinator do?

A clinical data coordinator is responsible for overseeing a number of data related tasks associated with running a clinical facility. In this career, your job duties include creating reports on patient data, developing programs that support a clinical study, and providing information to ensure regulatory compliance on behalf of the clinic. The qualifications needed to have a career as a clinical data coordinator include a bachelor's degree in computer science or a related field. You also need strong analytical skills and experience working with databases.

How does a clinical data coordinator typically collaborate with other teams during a clinical trial?

Clinical Data Coordinators work closely with clinical research associates, data managers, and regulatory teams to ensure the accurate collection and management of trial data. They frequently communicate with site staff to resolve data discrepancies and ensure adherence to protocol and data quality standards. Regular meetings and updates are common to address ongoing data queries, share progress, and align on timelines. This cross-functional collaboration is vital for maintaining the integrity of clinical trial data and supporting successful study outcomes.

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

To thrive as a Clinical Data Coordinator, you need strong analytical skills, attention to detail, and a background in life sciences or a related field, often supported by a bachelor’s degree. Familiarity with clinical data management systems (CDMS), electronic data capture (EDC) tools, and knowledge of regulatory standards such as GCP and FDA guidelines are essential. Excellent organizational skills, effective communication, and the ability to collaborate with multidisciplinary teams help set top candidates apart. These competencies ensure accurate data collection and integrity, which are crucial for the success and compliance of clinical trials.

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

AspectClinical Data CoordinatorClinical Research Associate
Primary RoleManage and ensure accuracy of clinical data collection and entryOversee clinical trial sites, monitor study progress, and ensure compliance
Required CredentialsTypically a bachelor's degree in health, life sciences, or related fieldUsually a bachelor's degree in health sciences, along with monitoring certifications
Work EnvironmentData management teams, clinical trial databases, research organizationsClinical sites, monitoring visits, regulatory agencies
Industry UsageCommon in clinical data management and research organizationsCommon in pharmaceutical companies and contract research organizations

The Clinical Data Coordinator focuses on managing and verifying clinical data accuracy, while the Clinical Research Associate monitors trial sites and ensures compliance. Both roles are essential in clinical research but differ in daily responsibilities and focus areas.

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

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

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

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

Infographic showing various Clinical Data Coordinator job openings in Riverside, CA as of August 2026, with employment types broken down into 94% Full Time, and 6% Part Time. Highlights an 100% In-person job distribution, with an average salary of $64,334 per year, or $30.9 per hour.

$92K - $130K/yr

Full-time

Re-posted 23 days ago


Edwards Lifesciences rating

8.3

Company rating: 8.3 out of 10

Based on 30 frontline employees who took The Breakroom Quiz

68th of 540 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.

Aortic stenosis impacts millions of people globally, yet it often remains under-diagnosed and under-treated. Edwards' groundbreaking work in transcatheter aortic heart valve replacement (TAVR) pioneered an innovative, life-changing solution for patients by offering heart valve replacement without the need for open heart surgery. Our Transcatheter Heart Valve (THV) business unit continues to partner with cardiologists and clinical teams to transform patient care with devices supported by clinical evidence. It's our driving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey.

How you will make an impact:

  • Identifying technical and data issues and collaborating with appropriate team members to bring to resolution; Determining root cause and recommending and implementing corrective actions.
  • Analyzing clinical output of highly complex studies and providing high level summary with supporting details of study trial status (e.g., Core Lab image perspective) to stakeholders and clinical trial management.
  • Identifying, developing, recommending, and leading implementation of complex process development and process improvement solutions to optimize global trial workflow timelines, (e.g., open information requests, aging issues, status of image analysis from Core Labs to study database, etc.).
  • Providing guidance and representing department to communicate risk and impact to study core team's key milestones and deliverables.
  • Developing timeline assessment (e.g., clinical site through image transfer vendor to Independent Core Lab) in collaboration with clinical stakeholders in order to meet key study milestones and deadlines.
  • Developing training material content in collaboration with clinical stakeholders for clinical sites and clinical field staff.
  • Assessing knowledge and/or quality gaps of clinical staff and determining appropriate training plans and/or needs in collaboration with management.

What you'll need (Required):

  • Bachelor's Degree in related field with 5 years of previous hands-on clinical research related experience.

What else we look for (Preferred):

  • Excellent computer skills in usage of MS Office Suite including Excel and MS Project
  • Excellent written and verbal communication skills and interpersonal relationship skills including consultative and relationship management skills
  • Excellent problem-solving and critical thinking skills
  • Full understanding and knowledge of principles, theories, and concepts relevant to clinical trial management
  • Full knowledge of human anatomy and physiology
  • Excellent problem-solving, organizational, analytical and critical thinking skills
  • Good leadership skills and ability to influence change
  • 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 inter-departmental teams and key contact representing the organization on contracts or projects
  • Ability to interact with senior internal and external personnel, inclusive of key opinion leaders (KOL) on significant matters often requiring coordination between organizations

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.
For California, the base pay range for this position is $92,000 to $130,000 (highly experienced).
The pay for the successful candidate will depend on various factors (e.g., 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.


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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