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Clinical Research Rater Jobs (NOW HIRING)

Wake Research

Clinical Research Coordinator

Irvine, CA

$30 - $40/hr

The Clinical Research Coordinator (CRC) is a specialized research professional working with and ... This position offers a competitive pay rate of $30-$40 per hour. *M3 reserves the right to change ...

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How much do clinical research rater jobs pay per hour?

As of Jun 16, 2026, the average hourly pay for clinical research rater in the United States is $22.71, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $25.96 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Clinical Research Rater position, and why are they important?

To thrive as a Clinical Research Rater, you need a background in psychology, neuroscience, or a related health science field, with strong attention to detail and standardized assessment skills. Familiarity with clinical trial protocols, electronic data capture systems, and rating scales like the Hamilton Depression Rating Scale or PANSS is often required. Excellent observational, interpersonal, and communication skills help you accurately assess participants and collaborate with multidisciplinary research teams. These abilities ensure precise data collection and reporting, which are critical for the validity and success of clinical research studies.

What is a Clinical Research Rater job?

A Clinical Research Rater is responsible for administering standardized assessments and interviews to clinical trial participants to evaluate their cognitive, psychiatric, or neurological status. They work closely with investigators and study coordinators to ensure data accuracy and consistency in clinical trials. Raters must be trained in administering rating scales and maintaining objectivity in their evaluations. This role is critical in ensuring the integrity of clinical trial outcomes, especially in studies related to mental health, neurology, and other therapeutic areas.

What are some typical challenges faced by Clinical Research Raters in their daily work?

Clinical Research Raters often face the challenge of maintaining objectivity and consistency while administering complex assessments across diverse participant populations. They must carefully follow study protocols, manage detailed documentation, and adapt to changes in trial requirements or participant schedules. Working closely with other research staff and clinicians requires strong communication and teamwork, especially when addressing discrepancies or unexpected findings. Staying up to date with assessment tools and best practices helps minimize errors and supports the integrity of the study data.

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Clinical Research Rater jobs near you
Infographic showing various Clinical Research Rater job openings in the United States as of June 2026, with employment types broken down into 2% Internship, 85% Full Time, 9% Part Time, 2% Temporary, and 2% Contract. Highlights an 91% In-person, 2% Hybrid, and 7% Remote job distribution, with an average salary of $47,241 per year, or $22.7 per hour.
Clinical Rater, Neurology

Clinical Rater, Neurology

Tandem Clinical Research

Marrero, LA • On-site

Full-time

Posted 17 days ago

Job description

Job Type
Full-time
Description
Job Description Full-Time On-Site
Position Summary
The Clinical Rater is responsible for interviewing research participants and their informants or caregivers who are being evaluated for enrollment in clinical studies across a range of health conditions. Working as part of a multidisciplinary research team, this role administers and scores protocol-specified psychometric rating scales, ensures participant safety, and maintains data integrity in full compliance with study protocols, SOPs, GCP, ICH guidelines, and applicable FDA regulations.
This position plays a key role in the accuracy and consistency of clinical trial data by preventing rater drift, completing all sponsor-required certifications, and supporting the Principal Investigator in determining participant eligibility.
Key Responsibilities
Participant Screening & Assessment
  • Review subject medical histories and conduct pre-screening interviews to assess eligibility for specific clinical trials
  • Administer protocol-specified psychometric rating scales for participants across a wide range of diagnoses, including Alzheimer's Disease, Mild Cognitive Impairment, MDD, Anxiety Disorders, ADHD, Bipolar Disorder, PTSD, Schizophrenia/Schizoaffective Disorder, and Substance Use Disorders
  • Calculate and apply rating scale results to determine protocol eligibility under the supervision of the Principal Investigator
  • Conduct telephone pre-screens and eligibility interviews as needed

Data Integrity & Documentation
  • Maintain accurate, complete, and timely source documentation in accordance with ALCOA-C standards
  • Complete all sponsor- and monitor-assigned queries within required timeframes
  • Actively work to maintain consistency in rating performance over time for individual subjects to prevent rater drift
  • Maintain strict confidentiality of participant and company information in compliance with HIPAA guidelines

Participant Safety & Communication
  • Ensure participant safety by appropriately assessing and responding to any potential for harm to self or others identified during evaluations, and reporting per company policy
  • Provide appropriate community resource referrals to participants, caregivers, and family members as needed
  • Facilitate timely, professional communication with participants, study staff, Sponsors, CROs, Monitors, Auditors, and central rating organizations
  • Articulate rating concerns or issues to the CRO, Sponsor, Principal Investigator, and study team

Team Leadership & Training
  • Serve as study lead across a minimum of four concurrent studies
  • Provide weekly schedule oversight for a minimum of two study coordinators
  • Complete all Sponsor-assigned rater training and maintain certification and re-certification per protocol requirements
  • Attend Sponsor meetings, Monitor visits, webinars, and company training programs
  • Perform additional duties as assigned

Ideal Candidate Profile
Someone who:
  • Understands how rigorous, consistent ratings directly impact clinical trial outcomes
  • Notices when a participant interaction is off-protocol and proactively corrects course
  • Is comfortable working across research, clinical, and sponsor-facing teams without close supervision
  • Brings genuine empathy and professionalism when working with participants of varying cognitive abilities
  • Takes ownership of rater certification, re-certification, and quality standards

Requirements
Required Qualifications
  • Minimum Bachelor's degree (B.A. or B.S.) in Psychology, Neuroscience, or a closely related field
  • At least 2 years of experience administering psychometric rating scales in a clinical or clinical trial setting, or an equivalent combination of education and experience
  • Solid working knowledge of clinical research protocols, FDA regulations, GCP, and ICH guidelines
  • Experience conducting cognitive and clinical assessments with adult and/or geriatric populations
  • Strong documentation skills with demonstrated attention to detail
  • Proficiency with Microsoft Office, EHR platforms, email, and web-based applications; 40+ WPM typing
  • Strong written and verbal communication skills and ability to work cross-functionally

Preferred Qualifications
  • Master's degree in Psychology, Neuroscience, or a related field; Certified Psychometrist designation is a plus
  • Current or prior certification in one or more of the following scales: MMSE, MoCA, ADAS-Cog, CDR / CDR-SB, RBANS, ADCS-ADL, NPI, MDS-UPDRS, Hoehn & Yahr, PDQ-39, C-SSRS, CGI-S / CGI-I/ ADCS-CGIC, PGI-S, ISI, PSQI, ESS, MSLT, NSS, TETRAS, TFC
  • Bilingual proficiency in English and Spanish
  • BLS certification
  • Experience supervising or mentoring junior staff in a clinical research environment

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