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Full Time Clinical Research Rater Jobs (NOW HIRING)

Research Centers of America

Clinical Rater

Hollywood, FL · On-site

... Research also provides highly competitive compensation and a generous benefits package to full time ... Administers clinical rating scales on study participants to confirm diagnosis and determine current ...

University of Miami

Clinical Research Coordinator 1

Miami, FL · On-site

$23.25 - $30.75/hr

Clinical Research Coordinator 1 The University of Miami/UHealth department of Neurology has an exciting opportunity for a Full Time Clinical Research Coordinator 1 to work at the UHealth Medical ...

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How much do full time clinical research rater jobs pay per hour?

As of Jun 22, 2026, the average hourly pay for full time 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 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 key skills and qualifications needed to thrive as a Full Time Clinical Research Rater, and why are they important?

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 Full Time Clinical Research Raters?

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.
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Full Time Clinical Research Rater jobs near you
Infographic showing various Full Time Clinical Research Rater job openings in the United States as of June 2026, with employment types broken down into 88% Full Time, and 12% Part Time. Highlights an 78% Physical, 6% Hybrid, and 16% Remote job distribution, with an average salary of $47,241 per year, or $22.7 per hour.

Clinical Rater, Neurology

Prolerity Clinical Research

Marrero, LA • On-site

Full-time

Posted 23 days ago

Job description

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