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Clinical Research Rater Remote Jobs in California

NCIRE

Staff Research Associate I

San Francisco, CA · Remote

... clinical and experimental studies on trauma- and stressor-related disorders in Veterans , with a ... heart rate (HR), heart rate variability (HRV), facial coding outputs, and remote ...

Headlands Research

Pharmacy Technician

San Diego, CA · On-site +1

$18.50 - $22.50/hr

San Diego, CA Artemis Institute for Clinical Research Full-time | Onsite (no opportunities for hybrid or remote) For experienced Pharmacy Technicians looking for meaningful work in clinical research.

IQVIA

Freelance Independent Rater

San Francisco, CA · Remote

$62K - $156K/yr

... LI-Remote #LI-HCPN IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create ...

New

IQVIA

Freelance Independent Rater

San Francisco, CA · Remote

$62K - $156K/yr

... LI-Remote #LI-HCPN IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create ...

New

IQVIA

Freelance Independent Rater

Los Angeles, CA · Remote

$62K - $156K/yr

... LI-Remote #LI-HCPN IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create ...

New

IQVIA

Freelance Independent Rater

Los Angeles, CA · Remote

$62K - $156K/yr

... LI-Remote #LI-HCPN IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create ...

New

CareDx, Inc.

Clinical Trial Manager

Brisbane, CA · Remote

Minimum of 4 years of clinical trial management and 2+ years clinical research associate with on-site/remote clinical monitoring experience in the biotechnology/pharmaceutical/CRO industry. * Minimum ...

Tilda Research

About Tilda Research We are a clinical trial network built from the ground up, suitable for the ... Remote first * Flexible PTO and hours Employment Type: FULL_TIME

Intuitive

Senior Clinical Study Manager

Sunnyvale, CA · On-site +1

Oversee 3rd parties and/or clinical research organizations (CROs), as applicable * Perform on-site and remote site qualification visits, site initiation visits, interim monitoring visits and site ...

YO AI Labs

Biostatistician Expert - Remote

San Jose, CA · Remote

$60 - $70/hr

Remote Job Type: Contractor Pay: $60-$65/hour Job Overview We are looking for an experienced Biostatistician to support clinical research projects by analyzing clinical trial data, validating ...

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All JobsClinical Research Rater JobsClinical Research Rater Remote JobsClinical Research Rater Remote Jobs in California

Clinical Research Rater Remote information

What is a clinical research rater?

A Clinical Research Rater (Remote) is a professional who works from a remote location to assess and evaluate participants in clinical research studies. They are responsible for administering psychological or cognitive assessments, interviews, and questionnaires to study subjects according to research protocols. The data they collect is used to determine the effectiveness and safety of medical treatments or interventions being studied. This position requires strong attention to detail, excellent communication skills, and the ability to follow standardized procedures. Remote raters typically collaborate with research teams via secure digital platforms and may require specific certifications or training.

What are the key skills and qualifications needed to thrive as a clinical research rater?

To thrive as a Clinical Research Rater (Remote), you need a background in psychology, neuroscience, or a related field, along with experience in clinical research and administering standardized assessments. Familiarity with electronic data capture (EDC) systems, clinical trial protocols, and certifications such as Good Clinical Practice (GCP) are highly valued. Attention to detail, strong organizational skills, and the ability to communicate clearly with research teams are crucial soft skills. These abilities ensure accurate data collection, adherence to study protocols, and high-quality research outcomes in a remote environment.

What are some typical challenges faced by remote clinical research raters, and how can they be addressed?

Remote Clinical Research Raters often face challenges such as maintaining consistent communication with study teams and ensuring accurate, unbiased assessments when working independently. To address these, it's important to establish clear protocols for virtual collaboration, regularly attend team meetings, and utilize secure data management systems. Staying organized and proactively reaching out for clarification when needed can help maintain high-quality data collection and foster a supportive remote work environment.

What is the difference between Clinical Research Rater Remote vs Clinical Data Entry Specialist?

AspectClinical Research Rater RemoteClinical Data Entry Specialist
Required credentialsHigh school diploma or equivalent; some roles may require clinical or research experienceHigh school diploma or equivalent; data entry skills preferred
Work environmentRemote, flexible hours, often part-timeRemote or on-site, regular hours, often full-time
Employer and industry usagePharmaceutical companies, research organizations, clinical trial sitesHealthcare providers, research organizations, hospitals

While both roles involve working remotely in the healthcare and research industry, Clinical Research Rater Remote focuses on evaluating patient data and clinical outcomes, whereas Clinical Data Entry Specialists primarily input and manage clinical data. The roles differ in responsibilities, with the former emphasizing assessment and analysis, and the latter concentrating on data accuracy and entry.

What are the most commonly searched types of Clinical Research Rater jobs in California?

The most popular types of Clinical Research Rater jobs in California are:

What are popular job titles related to Clinical Research Rater Remote jobs in California?

For Clinical Research Rater Remote jobs in California, the most frequently searched job titles are:

What job categories do people searching Clinical Research Rater Remote jobs in California look for?

The top searched job categories for Clinical Research Rater Remote jobs in California are:

What cities in California are hiring for Clinical Research Rater Remote jobs?

Cities in California with the most Clinical Research Rater Remote job openings:

Clinical Research Rater Remote jobs near you
Infographic showing various Clinical Research Rater Remote job openings in California as of August 2026, with employment types broken down into 2% As Needed, 73% Full Time, 17% Part Time, 2% Temporary, and 6% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution.

Sr. Clinical Research Associate (US)

Alimentiv

San Francisco, CA • On-site, Remote

Full-time

This job post has expired today. Applications are no longer accepted.

Job description

Independently performs, coordinates and oversees all aspects of the clinical site monitoring services, assessing protocol and regulatory compliance as per Alimentiv's and sponsor's standard processes, ICH/GCP guidelines and local regulation. Serves as the primary liaison between the sponsor/Alimentiv and investigative sites by playing a critical role in the execution of clinical study plans. Provides guidance and mentoring CRA I and II, collaborating effectively with cross-functional stakeholders in a dynamic, results-driven and high-accountability environment. Perform CRA Assessment Visits and participate in audits/inspections, when required.
Site Monitoring activities (55-60%)
  • Independently conduct and document onsite and remote activities, including site monitoring and close-out visits. Ensure that all activities are documented in accordance with applicable SOPs and study guidance.
  • Collaborate with site staff to review and ensure that the data reported in the applicable study system(s) is consistent with the source documents and compliant with study requirements.
  • Monitor, resolve and/or facilitate resolution of data queries and escalate issues as appropriate.
  • Coordinate the shipment of clinical supplies, including but not limited to, investigational product, laboratory supplies, ePROs and study documents.
  • Ensures site staff is trained in all aspects of the study including but not limited to the protocol, study plans, systems and ICH-GCP.
  • Participate in routine study progress meetings, teleconferences, and Investigator's meetings.
  • Routinely review ISF and TMF for accuracy, timeliness, and completeness. Request documents from the site, as required.

Site Management activities (15-20%)
  • Act as a primary contact for any questions or issues that arise from investigational sites.
  • Oversee overall integrity of the study and promote positive working relationships with the site staff and study team members.
  • Facilitate and support site staff with access to study systems and ensure sites are compliant with project specific training requirements.
  • Ensure all site related issues are followed until resolution, including action items and protocol deviations.
  • Coordinate delivery of clinical sites communications, collaborating with project teams, to ensure investigational sites are provided accurate ongoing data, updates, information and feedback on project/regulatory guidelines and objectives throughout the project lifecycle.
  • Regularly review the study related systems remotely to ensure compliance, accuracy and completeness.
  • Translate site documents for TMF filing when applicable.
  • Routinely review the TMF for accuracy, timeliness, and completeness. Request documents from the site, as required.
  • Coordinate the shipment of clinical supplies, including but not limited to, investigational product, laboratory supplies, ePROs and study documents.
  • Participate in audits/inspections and follow-up on issues and implement actions, when required.
  • Participate in routine study progress meetings and teleconferences.

Site Recruitment and Setup (15-20%)
  • Identify and advise on site investigators selection, independently conduct and document onsite and remote activities, including site qualification and initiation visits. Ensure that all activities are documented in accordance with applicable SOPs and study guidance.
  • Coordinate the shipment and delivery of clinical supplies, including but not limited to laboratory supplies, study documents and investigational product.
  • Responsible for all site management activities related to site activation and work with the sites to meet clinical project timelines and milestones.
  • Support the study Start-up team by following up on pending documents, as needed.
  • Support the Regulatory team by reviewing, localizing and translating site documents, as required.
  • Optimize patient recruitment providing guidance and support to site teams to meet the site recruitment milestones.
  • Participate in Investigator's meetings.

Mentoring and Internal Initiatives (5-10%)
  • Mentor and support CRA I and II.
  • Perform CRA Assessment Visits, co-monitoring visits or visit sign-off process, providing feedback.
  • Assist the MSM hiring Manager by participating in interviews with candidates for the CRA position, as requested.
  • Participate in process improvement initiatives and contribute to the development of best practices.

Qualifications
  • The successful candidate will possess a minimum of a college diploma/degree and 4-6 years of related experience.
  • Ability to regularly travel to sites.
  • Proficient in using EDC systems (e.g., Medidata Rave, Oracle InForm), IRT, eTMF, CTMS, and Microsoft Office Suite.
  • Ability to travel up to 40-60%, depending on project assignment and geographic location of sites.
  • Strong interpersonal and problem-solving skills; able to work independently and within cross-functional teams.
  • Great communication and organizational skills, detailed orientation and sense of urgency are required.

Working Conditions
  • Home-based
  • Regular travel is required

$86,000 - $143,000 a year
+bonus
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