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Full Time Clinical Research Rater Jobs in California

Amicis Research Center

Be Seen First

Clinical Research Coordinator

Santa Clarita, CA · On-site

$25 - $40/hr

We are seeking a dedicated and detail-oriented Clinical Research Coordinator to join our team. This ... Job Type: Full-time Pay: $25.00 - $40.00 per hour Expected hours: 40 per week Benefits: * Dental ...

Headlands Research

Clinical Research Manager

Escondido, CA · On-site

$100K - $105K/yr

At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities ... Position Type: Full-time Location: Onsite in Escondido, CA Responsibilities: * Clinical Trial ...

Headlands Research

Clinical Research Manager

Escondido, CA · On-site

$100K - $105K/yr

At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities ... Position Type: Full-time Location: Onsite in Escondido, CA Responsibilities: * Clinical Trial ...

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Full Time Clinical Research Rater information

What is a full time clinical research rater?

Full Time Clinical Research Raters are professionals who assess and document the progress, symptoms, and responses of patients participating in clinical research studies. They use standardized rating scales, interviews, and questionnaires to collect accurate data that helps determine the effectiveness and safety of new treatments or interventions. These raters play a vital role in ensuring the integrity and quality of clinical trial data, often working closely with clinicians, researchers, and study coordinators. Their responsibilities also include adhering to study protocols, maintaining patient confidentiality, and ensuring compliance with regulatory standards.

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

Success as a Full Time Clinical Research Rater requires a background in psychology, neuroscience, or a related field, along with experience in clinical assessments and data collection. Familiarity with standardized rating scales, clinical trial databases, and regulatory compliance systems like Good Clinical Practice (GCP) certification is typically expected. Strong attention to detail, interpersonal communication, and objective judgment are crucial soft skills for accurate participant evaluation and collaboration with research teams. These competencies ensure reliable data collection, regulatory adherence, and the integrity of clinical research outcomes.

What are some typical challenges a full time clinical research rater may encounter, and how can they be managed?

Full Time Clinical Research Raters often face challenges such as managing large volumes of patient assessments, maintaining objectivity during subjective ratings, and adhering to strict study protocols. Balancing accuracy with efficiency is key, especially when dealing with sensitive patient information and tight study timelines. Collaborating closely with investigators and other research staff, participating in regular trainings, and using standardized rating tools can help ensure consistency and reliability in data collection.

What is the difference between Full Time Clinical Research Rater vs Part Time Clinical Research Rater?

AspectFull Time Clinical Research RaterPart Time Clinical Research Rater
Work HoursTypically 35-40 hours per weekLess than 20 hours per week
CertificationsOften requires relevant healthcare or research certificationsMay require similar certifications but less emphasis
Work EnvironmentFull-time employment in research facilities or remotePart-time roles, flexible locations
Employer UsageMajor research organizations, pharmaceutical companiesFreelance or contract research organizations

The main difference between a Full Time Clinical Research Rater and a Part Time Clinical Research Rater lies in work hours, certification emphasis, and employment type. Full-time roles offer consistent hours and benefits, while part-time positions provide flexibility. Both roles involve evaluating clinical data, but full-time positions are more integrated into research teams.

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 Full Time Clinical Research Rater jobs in California?

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

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

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

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

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

Full Time Clinical Research Rater jobs near you
Infographic showing various Full Time Clinical Research Rater job openings in California as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution.

Clinical Scientist/Neuropsychological Rater

Irvine Clinical Research

Los Angeles, CA • On-site

$85K/yr

Full-time

Re-posted 5 days ago

Job description

Irvine Clinical Research, a research site specializing in late phase CNS clinical trials, is seeking applicants for a Clinical Scientist in our enrollment core. The clinical scientist will work on prescreening and screening potential candidates for outpatient Phase II/III clinical trials in Neurology and Psychiatry. Study participants are generally adults with concerns about memory (e.g. MCI and Early-Mild AD), although our site also conducts research on drugs to treat depression and other illnesses.
Job Duties
  • Assess potential and returning study participants using clinical judgement as well as psychological, neurological, and psychiatric clinical rating scales
  • Conduct clinical interviews to collect psychological/medical information and to effectively screen potential participants for appropriate research opportunities at our centers
  • Educate participants about the potential benefits and risks of our clinical trials through the informed consent process and outreach events
  • Communicate with investigators, coordinators, and study teams about participants
  • Assist with scientific initiatives, study operations, and participant enrollment as needed
Job Requirements
  • MA/MS/MSW/PhD/PsyD in psychology, neuroscience, or related field
  • Experience with cognitive assessments and/or experience working with older adults with memory concerns, Mild Cognitive Impairment, or Early/Mild/Moderate Alzheimer’s Disease
  • A command of professional spoken and written English
The starting salary for this position is approximately $85,000 per year. Higher salary is negotiable with candidates who have experience with Psychometrician / Psychological Rater experience in pharmaceutical clinical trials.
 
This is a full-time employment position based in-person at one of our clinics.
 
The company pays for 100% of health/dental/vision individual insurance costs for eligible full-time employees. Vacation (PTO) is earned at a rate of 3 weeks per year.