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Home Based Human Subject Research Jobs in Riverside, CA

Alimentiv

Statistician

Ontario, CA · Remote

Act as subject matter expert, providing statistical support to project teams, quality/study ... Home-based. $78,000 - $130,000 a year + Annual Bonus - Target 8% Extended Health Benefits

City of Hope

Clin Research Nurse - BSN - OC

Irvine, CA · On-site

... home) including triage of phone calls and proactive patient communication. You will educate ... Human subjects protection training (can be completed after hire) * Current California RN License

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All JobsHome Based Human Subject Research JobsHome Based Human Subject Research Jobs in Riverside, CA

Home Based Human Subject Research information

See Riverside, CA salary details

$13

$24

$30

How much do home based human subject research jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for home based human subject research in Riverside, CA is $24.40, according to ZipRecruiter salary data. Most workers in this role earn between $20.05 and $29.62 per hour, depending on experience, location, and employer.

What is home based human subject research?

Home based human subject research refers to scientific studies involving human participants that are conducted primarily in the participants’ homes rather than in a laboratory or clinical setting. This type of research often utilizes remote monitoring, online surveys, telehealth consultations, or mailed testing kits to collect data. It allows for greater participant comfort, convenience, and accessibility, while also enabling researchers to study real-world behaviors and outcomes. However, it requires careful attention to participant privacy, informed consent, and data security.

What are the key skills and qualifications needed to thrive in home based human subject research?

To thrive in Home-Based Human Subject Research, you need a solid background in research methodology, data collection, and ethical compliance, often supported by a degree in a relevant field and training in human subjects protection. Familiarity with survey platforms, remote data collection tools, and Institutional Review Board (IRB) processes is typically required. Strong communication, attention to detail, and organizational skills are crucial for building rapport with participants and managing study protocols remotely. These skills and qualifications are essential to ensure ethical, accurate, and effective research outcomes while maintaining participant trust and data integrity.

What is the difference between Home Based Human Subject Research vs Clinical Research Coordinator?

AspectHome Based Human Subject ResearchClinical Research Coordinator
CredentialsOften requires research ethics training, basic healthcare knowledgeRequires clinical research certifications, healthcare or science background
Work EnvironmentPrimarily remote, conducting studies from homeTypically in clinics, hospitals, or research sites
Employer & IndustryResearch institutions, universities, healthcare companiesPharmaceutical companies, hospitals, research organizations
Job FocusRecruiting and monitoring human subjects remotely for studiesManaging clinical trials, coordinating study activities

Home Based Human Subject Research involves conducting research with participants remotely, often from home, focusing on recruiting and monitoring subjects. In contrast, Clinical Research Coordinators work onsite managing clinical trials directly at research sites. Both roles require knowledge of research protocols, but the environment and daily tasks differ significantly.

What are some common challenges faced by home based human subject researchers, and how can they be addressed?

Home-based human subject researchers often face challenges such as maintaining participant engagement remotely, ensuring data privacy, and adhering to ethical guidelines without in-person supervision. Building strong communication channels, using secure data collection tools, and regularly consulting with institutional review boards can help address these concerns. Additionally, staying organized and proactive in scheduling virtual meetings can foster trust and compliance among participants, ensuring research quality and integrity.
What are the most commonly searched types of Human Subject Research jobs in Riverside, CA? The most popular types of Human Subject Research jobs in Riverside, CA are:
What are popular job titles related to Home Based Human Subject Research jobs in Riverside, CA? For Home Based Human Subject Research jobs in Riverside, CA, the most frequently searched job titles are:
What job categories do people searching Home Based Human Subject Research jobs in Riverside, CA look for? The top searched job categories for Home Based Human Subject Research jobs in Riverside, CA are:
What cities near Riverside, CA are hiring for Home Based Human Subject Research jobs? Cities near Riverside, CA with the most Home Based Human Subject Research job openings:
Home Based Human Subject Research jobs near you
Infographic showing various Home Based Human Subject Research job openings in Riverside, CA as of August 2026, with employment types broken down into 82% Full Time, and 18% Part Time. Highlights an 94% In-person, and 6% Remote job distribution, with an average salary of $50,752 per year, or $24.4 per hour.

Clinical Research Site Manager

Headlands Research

Riverside, CA • On-site

Full-time

PTO

Re-posted 5 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

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