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Research Data Director Jobs in Riverside, CA (NOW HIRING)

Sr. Data Engineer

Highland, CA · On-site

$113K - $136K/yr

... research data to support organizational decision-making. This position is onsite 5 days per week in ... Related, relevant, and/or direct experience may be considered in lieu of minimum educational ...

Influences without direct authority, using data and evidence to drive aligned, mutually beneficial ... Must have 6+ years of pharma / clinical research / data management / health care experience or 8+ ...

... ​Influences without direct authority, using data and evidence to drive aligned, mutually ... Must have 6+ years of pharma / clinical research / data management / health care experience or 8+ ...

Stand up a Data, AI & Analytics Center of Excellence with domainaligned product squads (M&Q, R&D ... direct your inquiries to our HR Department (flbi@fujifilm.com). Employment Type: OTHER

Director Data AI & Analytics

Irvine, CA · On-site

$154.57 - $216.10/hr

Stand up a Data, AI & Analytics Center of Excellence with domain-aligned product squads (M&Q, R&D ... direct your inquiries to our HR Department (flbi@fujifilm.com). #J-18808-Ljbffr

New

Director Master Data Management

Irvine, CA · On-site +1

$143K - $228K/yr

The role partners closely with Supply Chain, Finance, Commercial, R&D, Quality, and IT functions to ... Data influential leadership experience is required * 3+ years of direct people leadership is ...

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Research Data Director information

See Riverside, CA salary details

$60K

$199.6K

$240.5K

How much do research data director jobs pay per year?

As of Aug 7, 2026, the average yearly pay for research data director in Riverside, CA is $199,598.00, according to ZipRecruiter salary data. Most workers in this role earn between $141,400.00 and $238,900.00 per year, depending on experience, location, and employer.

What are some common challenges faced by a research data director, and how can they be effectively addressed?

A Research Data Director often encounters challenges such as ensuring data integrity across multiple projects, managing compliance with institutional and federal data regulations, and coordinating data sharing among diverse research teams. Addressing these challenges requires strong leadership, the implementation of robust data governance frameworks, and ongoing training for staff on data best practices. Additionally, fostering open communication between researchers, IT, and compliance teams helps to proactively resolve issues and maintain smooth data operations.

What are the key skills and qualifications needed to thrive as a research data director?

To thrive as a Research Data Director, you need expertise in data management, statistical analysis, and research methodologies, typically supported by an advanced degree in a relevant field. Familiarity with data governance frameworks, statistical software (such as SAS, R, or SPSS), and compliance standards like HIPAA or GDPR is essential. Strong leadership, strategic thinking, and communication skills help guide teams and facilitate collaboration across departments. These skills ensure robust data integrity, drive impactful research outcomes, and maintain regulatory compliance in complex research environments.

What is a research data director?

Research Data Directors are professionals responsible for overseeing the management, organization, and integrity of data within research projects or institutions. They develop policies and strategies for data collection, storage, sharing, and security, ensuring compliance with ethical and legal standards. Research Data Directors often collaborate with researchers, IT teams, and administrators to facilitate data-driven decision-making and support high-quality research outcomes. Their role is vital for maintaining data quality, accessibility, and reproducibility in research environments.
What are the most commonly searched types of Research Data jobs in Riverside, CA? The most popular types of Research Data jobs in Riverside, CA are:
What job categories do people searching Research Data Director jobs in Riverside, CA look for? The top searched job categories for Research Data Director jobs in Riverside, CA are:
What cities near Riverside, CA are hiring for Research Data Director jobs? Cities near Riverside, CA with the most Research Data Director job openings:
Infographic showing various Research Data Director job openings in Riverside, CA as of August 2026, with employment types broken down into 97% Full Time, and 3% Part Time. Highlights an 97% In-person, and 3% Remote job distribution, with an average salary of $199,598 per year, or $96 per hour.

Clinical Research Site Manager

Headlands Research

Riverside, CA

Full-time

PTO

Re-posted 3 days ago


Job description

The Role

The Site Manager performs clinical research activities as a Clinical Research Coordinator while also serving as Manager of the site operations. The Site Manager owns meeting or exceeding financial targets, KPIs, and patient enrollment, as well as champions screening, patient retention, and partnering with other Headlands centralized departments or sites.

Position Type:  Full-time

Location:  Onsite in Riverside, CA

Responsibilities:

  • Strategic and Operational Management
    • Evaluates overall performance of the Site and recommends and implements processes and plans for improvement.
    • Responsible for maintaining a site calendar to ensure adequate enrollment for studies and coordination of employee PTO.
  • Staff Development and Management
    • Fosters a culture of excellence, teamwork, and innovation among site staff
    • Hires, trains, and mentors site staff, including Clinical Research Coordinators, Research Assistants, Administrative Assistants, Registered Nurses, support personnel, etc.
    • Partners with Human Resources and Management when hiring new employees for the site by reviewing candidate credentials, conducting interviews, and giving input about potential new hires
    • Supervises performance of other Clinical Research Coordinators, Research Assistants, and support staff at the Site
  • Quality Assurance & Compliance
    • Maintains up-to-date knowledge of all relevant regulatory guidelines and requirements
    • Ensures the site's compliance with FDA, ICH, and local regulatory agency regulations
  • Clinical Research Coordination
    • In addition to assuming management responsibilities as a Site Manager, this individual performs the duties of a Clinical Research Coordinator
    • Protects the rights, safety, and welfare of human subjects, follows Good Clinical Practice, and works cooperatively with others
    • Monitors study activities to ensure compliance with study protocols, with site policies, and with applicable federal, state, and local regulations
    • Oversee the planning, initiation, and execution of clinical trials at the site
    • Maintains required records of study activity including case report forms, drug dispensation records, and regulatory forms
    • Manages and optimizes patient recruitment and retention efforts
    • Assesses eligibility of potential subjects through methods such as screening interviews, reviews of medical records, and discussions with physicians and other healthcare professionals
    • Addresses any patient concerns or issues promptly and professionally
  • Documentation and Reporting
    • Documents findings and events in the CTMS platform and in other binders and platforms as directed
    • Reviews proposed study protocols to evaluate factors such as sample collection processes, data management plans, and potential subject risks
  • Performs other duties as assigned, including duties routinely performed by the Company's Research Assistants

 

Requirements:

  • 5+ years of experience as a delegated Clinical Research Coordinator on multiple phase 2-4 clinical research trials, simultaneously
  • Proficiency in FDA regulations governing clinical trials
  • Strong supervisory skills to lead research staff effectively
  • Ability to collect and manage research data accurately
  • Familiarity with documentation review processes in clinical research
  • Knowledge of medical terminology relevant to clinical trials management
  • IATA (dangerous goods handling)
  • GCP (Good Clinical Practice)
  • Strong communication skills with all members of the team.

Preferred Qualifications:

  • Bachelor's degree
  • Capability to perform phlebotomy procedures
  • CCRC or CCRP certified