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Remote Ethics Investigator Jobs in Riverside, CA

Diality

Clinical Research Associate

Irvine, CA · Remote

$120K - $135K/yr

... ethics documents, such as IRB/EC submissions, contracts, and site feasibility questionnaires ... Track and manage trial documentation, including but not limited to site contracts, investigator ...

Liberty Mutual

Staff Counsel

Ontario, CA · On-site +1

Description This role is primarily remote in the state of California except for required ... Develop, implement, and continuously refine advanced legal strategies for discovery, investigation ...

Liberty Mutual

Staff Counsel

Ontario, CA · On-site +1

Description This role is primarily remote in the state of California except for required ... Develop, implement, and continuously refine advanced legal strategies for discovery, investigation ...

All JobsEthics Investigator JobsRemote Ethics Investigator JobsRemote Ethics Investigator Jobs in Riverside, CA

Remote Ethics Investigator information

See Riverside, CA salary details

$33.4K

$78.6K

$136.7K

How much do remote ethics investigator jobs pay per year?

As of Sep 1, 2026, the average yearly pay for remote ethics investigator in Riverside, CA is $78,584.00, according to ZipRecruiter salary data. Most workers in this role earn between $54,800.00 and $102,800.00 per year, depending on experience, location, and employer.

What is a remote ethics investigator?

A Remote Ethics Investigator is a professional who conducts investigations into ethical concerns, misconduct, or compliance violations within an organization while working remotely. Their responsibilities typically include gathering evidence, interviewing involved parties, reviewing documents, and preparing reports on their findings. They play a crucial role in ensuring that organizations maintain ethical standards and comply with laws and regulations. Working remotely, they use digital tools and secure communication methods to perform their duties efficiently. This role is essential in today's increasingly virtual work environments, where ethical issues may arise across distributed teams.

What are the key skills and qualifications needed to thrive as a remote ethics investigator?

To thrive as a Remote Ethics Investigator, you need a strong background in investigative techniques, analytical reasoning, and a degree in law, compliance, or a related field. Familiarity with case management software, digital evidence tools, and relevant certifications such as Certified Fraud Examiner (CFE) or Certified Compliance & Ethics Professional (CCEP) is often required. Exceptional written communication, discretion, and critical thinking skills help you navigate sensitive investigations and deliver clear findings. These competencies are crucial to ensuring thorough, impartial investigations and maintaining organizational integrity from a remote environment.

What are some common challenges faced by remote ethics investigators, and how can they be addressed?

Remote Ethics Investigators often face challenges such as managing sensitive information securely, building rapport with interviewees virtually, and ensuring thorough investigations without on-site presence. To address these, investigators typically use secure communication platforms, maintain clear documentation, and schedule regular check-ins with stakeholders. Additionally, collaborating closely with HR and compliance teams helps ensure a comprehensive and effective investigative process, even while working remotely.

What is the difference between Remote Ethics Investigator vs Remote Research Coordinator?

AspectRemote Ethics InvestigatorRemote Research Coordinator
Required CredentialsEthics certifications, research ethics trainingResearch certifications, project management skills
Work EnvironmentReview boards, ethical compliance settingsStudy sites, data collection, participant coordination
Industry UsageAcademic, clinical research, biotechAcademic, clinical trials, healthcare research

The Remote Ethics Investigator primarily focuses on reviewing and ensuring ethical compliance in research projects, often working with ethics boards. In contrast, the Remote Research Coordinator manages the day-to-day operations of research studies, including participant recruitment and data collection. Both roles are essential in research settings but differ in responsibilities and required credentials.

What are the most commonly searched types of Ethics Investigator jobs in Riverside, CA?

The most popular types of Ethics Investigator jobs in Riverside, CA are:

What are popular job titles related to Remote Ethics Investigator jobs in Riverside, CA?

For Remote Ethics Investigator jobs in Riverside, CA, the most frequently searched job titles are:

What job categories do people searching Remote Ethics Investigator jobs in Riverside, CA look for?

The top searched job categories for Remote Ethics Investigator jobs in Riverside, CA are:

What cities near Riverside, CA are hiring for Remote Ethics Investigator jobs?

Cities near Riverside, CA with the most Remote Ethics Investigator job openings:

Remote Ethics Investigator jobs near you
Infographic showing various Remote Ethics Investigator job openings in Riverside, CA as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 19% Part Time, and 1% Contract. Highlights an 93% Physical, 1% Hybrid, and 6% Remote job distribution, with an average salary of $78,584 per year, or $37.8 per hour.

Clinical Research Associate

Diality

Irvine, CA • Remote

$120K - $135K/yr

Full-time

Re-posted 23 days ago

Job description

Description

Company & Job Overview:

The Clinical Research Associate (CRA) will support Clinical Operations in planning, coordinating, and executing Diality clinical trials in compliance with applicable regulations (e.g., FDA, ISO 14155, ICH-GCP). This position plays a key role in supporting research projects at Diality, combing responsibilities of site management and administrative trial support to ensure smooth and efficient study operations. 


As applicable, the CRA position works closely with clinical sites, internal departments (e.g., medical affairs, field service, clinical operations, clinical training and support), and external partners (Contract Research Organization, vendors) to ensure the quality and integrity of clinical data while maintaining adherence to study timelines.  


Responsibilities:


Clinical Trial Administration 

  • Assist with trial start-up, including preparing and submitting regulatory and ethics documents, such as IRB/EC submissions, contracts, and site feasibility questionnaires. 
  • Maintain and organize the Trial Master File (TMF) and ensure all essential documents are current, complete, and audit-ready. 
  • Track and manage trial documentation, including but not limited to site contracts, investigator agreements, financial disclosure forms, and training records. 
  • Monitor study progress by updating trackers and preparing study status reports for internal and external stakeholders. 


Site Management & Communication: 

  • Establish, Monitor and Control tasks required tasks for site start-up activities during clinical trials. 
  • Facilitate Communication Plan for clinical trial sites, including communications for internal Diality support teams  
  • Act as a point of contact for clinical trial sites regarding study-related questions and issues. 
  • Assist in managing site readiness, including regulatory and ethics submissions as needed, contract negotiations, and training. 
  • Monitor site performance and compliance with protocols, regulations, and study timelines. 
  • Support site readiness by ensuring all required study materials, such as investigator site files and study binders, are prepared and distributed. 
  • Assist in scheduling and coordinating investigator meetings, site initiation visits (SIVs), and other study-related activities 

Regulatory Compliance & Documentation: 

  • As needed, assist with timely and accurate submission of regulatory documents, including IRB/EC approvals and site files. 
  • Assist in writing and reviewing protocols, informed consent forms (ICFs), and other study-related documents. 

Clinical Monitoring: 

  • Perform remote monitoring activities such as source data verification (SDV) and data entry checks. 
  • Assist with monitoring safety reporting, adverse events (AEs), and serious adverse events (SAEs). 
  • Support quality assurance efforts by identifying protocol deviations and ensuring corrective actions. 

Study Support: 

  • Participate in the development of study tools, training materials, and site binders. 
  • Assist in vendor and contract management for study-related services (e.g., laboratories, CROs). 
  • Track study metrics, such as patient recruitment, site enrollment, and data collection timelines. 


General Support: 

  • Schedule and organize internal and external meetings, including drafting meeting agendas and minutes. 
  • Assist in the preparation of presentations to both internal and external stakeholders as needed. 
  • Support audit and inspection readiness by ensuring proper documentation and compliance with company SOPs and regulatory guidelines. 

Collaboration & Reporting: 

  • Collaborate with other Diality cross-functional teams, including regulatory, quality to ensure study compliance. 
  • Support data management activities with data cleaning and resolving queries as applicable. 
  • Prepare regular study updates, reports, and presentations for internal stakeholders.


Requirements

Required Skills & Abilities

  • Attention to detail and problem-solving skills to ensure data quality and compliance 
  • Strong organizational and time management skills. 
  • Excellent written and verbal communication abilities. 
  • Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.  
  • Ability to work independently and collaboratively in a fast-paced environment.


Education & Experience

  • Bachelor's degree in a life science, healthcare, or related field (e.g., biology, nursing, or biomedical engineering). 
  • 5+ years of clinical research experience at a Sponsor, preferably in medical devices. A combination of other relevant experience (e.g., site level/CRO research) may also apply. 
  • Familiarity with clinical trial regulations, including FDA, ISO 14155, and ICH-GCP. 
  • Previous experience in a medical device company or knowledge of device-specific regulatory pathways. 
  • Experience with managing remote monitoring activities or decentralized clinical trials. 
  • Nephrology experience is a plus.


Travel

  • This role is primarily office-based with occasional travel (up to 50%) to clinical sites and meetings as needed.


Apply