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

Kaygen

Spec 3, Clinical Research

Irvine, CA · On-site

Partner with Clinical Data Management, Clinical Operations, and field teams to support data review, query management, and issue resolution. * Participate in ongoing process evaluations and recommend ...

New

Kaygen Inc.

Spec 3, Clinical Research

Irvine, CA · On-site

Partner with Clinical Data Management, Clinical Operations, and field teams to support data review, query management, and issue resolution. Participate in ongoing process evaluations and recommend ...

New

Johnson & Johnson

Clinical Research Manager

Irvine, CA · Hybrid

Provide input on clinical data review to prepare data for statistical analyses and publications ... Manages work independently. Independently solves problems arising during clinical trial execution ...

Jj

Clinical Research Manager

Irvine, CA · Hybrid

Provide input on clinical data review to prepare data for statistical analyses and publications ... Manages work independently. Independently solves problems arising during clinical trial execution ...

Jj

Clinical Research Manager

Irvine, CA · On-site +1

Manages and oversees ordering, tracking, and accountability of investigational products and trial ... Is responsible for clinical data review to prepare data for statistical analyses and publications;

Johnson & Johnson

Clinical Research Manager

Irvine, CA · On-site +1

Manages and oversees ordering, tracking, and accountability of investigational products and trial ... Is responsible for clinical data review to prepare data for statistical analyses and publications;

Jj

Staff Clinical Research Scientist

Irvine, CA · On-site

Clinical Development & Research - Non-MD Job Category: Scientific/Technology All Job Posting ... management using publication tools and systems * Stays on top of current scientific data by ...

Diality

Clinical Research Associate

Irvine, CA · Remote

$120K - $135K/yr

The Clinical Research Associate (CRA) will support Clinical Operations in planning, coordinating ... Support data management activities with data cleaning and resolving queries as applicable.

New

Diality Inc

Clinical Research Associate

Irvine, CA · On-site

$120K - $135K/yr

The Clinical Research Associate (CRA) will support Clinical Operations in planning, coordinating ... Support data management activities with data cleaning and resolving queries as applicable.

New

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All JobsClinical Data JobsClinical Data Manager JobsClinical Data Manager Jobs in Riverside, CA

Clinical Data Manager information

See Riverside, CA salary details

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$59

$85

How much do clinical data manager jobs pay per hour?

As of Jul 15, 2026, the average hourly pay for clinical data manager in Riverside, CA is $59.64, according to ZipRecruiter salary data. Most workers in this role earn between $47.16 and $70.96 per hour, depending on experience, location, and employer.

What are some common challenges Clinical Data Managers face when working on multi-site clinical trials?

Clinical Data Managers often encounter challenges such as ensuring data consistency across different sites, managing large volumes of complex data, and coordinating with site staff to resolve discrepancies. They must also stay up-to-date with regulatory requirements and ensure timely data cleaning and database lock. Effective communication and strong organizational skills are essential to navigate these complexities and maintain high data quality throughout the study.

What degree do you need to be a Clinical Data Manager?

A Clinical Data Manager typically needs at least a bachelor's degree in a health-related field such as life sciences, nursing, or health informatics. Many employers prefer candidates with a master's degree or additional certifications in clinical research or data management. Strong knowledge of database tools and regulatory standards is also important for the role.

What are the key skills and qualifications needed to thrive as a Clinical Data Manager, and why are they important?

To thrive as a Clinical Data Manager, you need a solid understanding of clinical research processes, data management principles, and a degree in life sciences, computer science, or related fields. Expertise with clinical data management systems (CDMS), electronic data capture (EDC) tools, and familiarity with regulatory standards like CDISC and GCP are typically required. Attention to detail, problem-solving abilities, and effective communication distinguish top performers in this role. These skills ensure accurate, compliant data handling and seamless collaboration across clinical research teams, which are critical for successful clinical trial outcomes.

What does a Clinical Data Manager do?

A Clinical Data Manager is responsible for collecting, validating, and managing data from clinical trials to ensure its accuracy, integrity, and compliance with regulatory standards. They design data collection systems, oversee database development, and collaborate with clinical research teams to resolve data discrepancies. By ensuring high-quality data, Clinical Data Managers play a vital role in the success of clinical trials and the development of new medical treatments.

What does a clinical data management do?

A clinical data manager is responsible for designing, implementing, and maintaining systems to collect, clean, and analyze data from clinical trials. They ensure data accuracy, integrity, and compliance with regulatory standards using tools like electronic data capture (EDC) systems. This role requires attention to detail, knowledge of Good Clinical Practice (GCP), and often involves collaboration with research teams and data analysts.

What Does a Clinical Data Manager Do?

A clinical data manager handles all the data needs of clinical trials for biotechnology and pharmaceutical companies. As a clinical data manager, your responsibilities include the research and storage of data related to clinical trials and programs. Your job duties are to collect, process, and analyze data. You must routinely evaluate your data collection and analysis processes to ensure that results are accurate and valid. You must also ensure that your work is in compliance with ethical research standards and regulations from organizations like the Food and Drug Administration (FDA).

How much does a Pfizer Clinical Data Manager make?

A Pfizer Clinical Data Manager typically earns between $80,000 and $120,000 annually, depending on experience, location, and level of responsibility. The role requires strong data management skills and familiarity with clinical trial software such as EDC systems.

What is the role of a Clinical Data Manager?

A Clinical Data Manager is responsible for designing, implementing, and maintaining systems to collect, manage, and ensure the quality of clinical trial data. They oversee data validation, perform data cleaning, and collaborate with study teams to ensure accurate and compliant data collection using tools like electronic data capture (EDC) systems. Their role is essential for supporting regulatory submissions and ensuring trial integrity.
More about Clinical Data Manager jobs
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 Manager jobs in Riverside, CA? For Clinical Data Manager jobs in Riverside, CA, the most frequently searched job titles are:
What job categories do people searching Clinical Data Manager jobs in Riverside, CA look for? The top searched job categories for Clinical Data Manager jobs in Riverside, CA are:
What cities near Riverside, CA are hiring for Clinical Data Manager jobs? Cities near Riverside, CA with the most Clinical Data Manager job openings:
Clinical Data Manager jobs near you
Infographic showing various Clinical Data Manager job openings in Riverside, CA as of July 2026, with employment types broken down into 94% Full Time, and 6% Contract. Highlights an 84% In-person, 6% Hybrid, and 10% Remote job distribution, with an average salary of $124,054 per year, or $59.6 per hour.
Spec 3, Clinical Research

Spec 3, Clinical Research

Kaygen

Irvine, CA • On-site

Other

Medical, Dental, Vision, Life, Retirement

This job post has expired 1 day ago. Applications are no longer accepted.

Job description

KAYGEN is an emerging leader in providing top talent for technology-based staffing services. We specialize in providing high-volume contingent staffing, direct hire staffing and project-based solutions to companies worldwide ranging from startups to Fortune 500 and Managed Service Providers (MSP) across a wide variety of industries.
The Clinical Research Specialist supports all phases of clinical studies, including study start-up, conduct, and closeout, with a primary focus on maintaining an audit- and inspection-ready Trial Master File (TMF). This role is responsible for organizing, reviewing, and maintaining clinical documentation within the Electronic Trial Master File (eTMF) and Clinical Trial Management System (CTMS) to ensure compliance with Good Clinical Practice (GCP), regulatory requirements, and company Standard Operating Procedures (SOPs). The Specialist collaborates with cross-functional teams to resolve documentation and data issues, supports audit readiness, and contributes to continuous process improvements that enhance operational efficiency and documentation quality.
Key Responsibilities

  • Support clinical trial start-up activities, including site readiness tracking, coordination of Site Qualification Visits (SQVs) and Site Initiation Visits (SIVs), and communication with investigative sites.
  • Assist with study conduct and closeout activities while ensuring all required documentation is complete and compliant.
  • Maintain, organize, and update study documentation within the eTMF and CTMS throughout the clinical trial lifecycle.
  • Review essential Trial Master File (TMF) documents for completeness, accuracy, and compliance with GCP, company SOPs, and applicable U.S. and international regulatory requirements.
  • Perform quality checks on clinical documentation to ensure inspection readiness for regulatory and quality audits, including FDA, PMDA, TUV, and other regulatory agencies.
  • Identify documentation inconsistencies, missing records, and compliance gaps; investigate issues and coordinate timely resolution with internal stakeholders.
  • Partner with Clinical Data Management, Clinical Operations, and field teams to support data review, query management, and issue resolution.
  • Participate in ongoing process evaluations and recommend improvements to enhance documentation quality, operational efficiency, and regulatory compliance.
  • Ensure adherence to Good Documentation Practices (GDP) and maintain accurate, organized, and audit-ready study records.
  • Support cross-functional collaboration to facilitate timely completion of clinical study deliverables
At KAYGEN, we are always looking for dynamic, talented and experienced individuals. We invite you to join our team of talented IT professionals, consulting at client locations across the globe. Our culture is team-orientated; we strive to stand by our core values of respect, honesty and integrity. Our team of experienced staffing experts will work with you to find you the best opportunity. For more information, please visit us at www.kaygen.com.
Benefits:
  • Free Healthcare Insurance
  • Vision and Dental Insurance
  • 401(k) Retirement Plan
  • Free Life Insurance
  • Sick Time Off
Achieve your Kaizen by clicking here. A unique and exclusive talent community supported by Kaygen, that includes programs like:
  • Certifications

  • Mentorship Program
  • Referrals
  • Family and Wellness benefits
  • Continuous Growth and Career Development

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