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Contract Investigator Jobs in Riverside, CA (NOW HIRING)

Diality Inc

Clinical Research Associate

Irvine, CA · On-site

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 ...

Diality

Clinical Research Associate

Irvine, CA · Remote

$120K - $135K/yr

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 ...

L3Harris Technologies

Intern, Contracts

Anaheim, CA

$21 - $41.50/hr

This role is responsible for assisting with proposal development, contract administration, and ... security investigation(s) and must meet eligibility requirements for access to classified ...

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Showing results 21-40

All JobsContract Investigator JobsContract Investigator Jobs in Riverside, CA

Contract Investigator information

See Riverside, CA salary details

$33.4K

$78.6K

$136.7K

How much do contract investigator jobs pay per year?

As of Sep 2, 2026, the average yearly pay for contract 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 contract investigator?

Contract investigators are professionals hired, often by government agencies or private companies, to conduct background checks, security clearance investigations, or other fact-finding assignments on a contractual basis. Their primary role is to gather and verify information about individuals, such as employment history, criminal records, and personal references, to determine eligibility for security clearances or employment. These investigators typically work independently, conducting interviews and reviewing documents, then compiling their findings into detailed reports for their clients. Contract investigators must follow strict guidelines and ethical standards to ensure the accuracy and confidentiality of the information they handle.

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

To thrive as a Contract Investigator, you need strong analytical abilities, attention to detail, and knowledge of investigative procedures, typically supported by a relevant bachelor's degree and background screening experience. Familiarity with case management systems, federal investigative standards, and sometimes specific certifications like OPM or DCSA credentialing is important. Excellent written communication, discretion, and interpersonal skills help in conducting interviews and compiling thorough reports. These skills are crucial to ensure accurate, ethical investigations that meet compliance and security standards.

What are some common challenges contract investigators face when conducting background checks, and how can they overcome them?

Contract Investigators often encounter challenges such as incomplete records, unresponsive sources, and tight deadlines when conducting background checks. To overcome these obstacles, it's important to maintain strong organizational skills, use a variety of verification methods, and communicate proactively with both clients and references. Building a network of reliable contacts and staying up to date on compliance requirements can also help ensure thorough and accurate investigations. Adaptability and persistence are key traits for success in this role.

What is the difference between Contract Investigator vs Insurance Investigator?

AspectContract InvestigatorInsurance Investigator
Required CredentialsTypically a background in law enforcement, criminal justice, or related fields; sometimes requires licensureOften requires a background in law enforcement, criminal justice, or insurance claims; licensure may be needed
Work EnvironmentFieldwork and office investigations, often on contract basis for private firms or government agenciesPrimarily fieldwork investigating insurance claims, sometimes in office settings
Employer & IndustryPrivate investigation firms, government agencies, legal firmsInsurance companies, third-party claims adjusters, legal firms

Both roles involve investigative work requiring similar credentials and environments. The main difference lies in their focus: Contract Investigators often handle legal or contractual investigations, while Insurance Investigators specialize in assessing insurance claims. Understanding these distinctions helps job seekers target the right opportunities in the investigation field.

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

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

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

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

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

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

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

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

Contract Investigator jobs near you
Infographic showing various Contract Investigator job openings in Riverside, CA as of August 2026, with employment types broken down into 85% Full Time, and 15% Part Time. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $78,584 per year, or $37.8 per hour.

Clinical Research Associate

Diality Inc

Irvine, CA • On-site

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