Clinical Rater, Neurology

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    "description_html": "<p>&nbsp;</p><p><em>Job Description &nbsp;| &nbsp;Full-Time | &nbsp;On-Site</em></p><p><strong>Position Summary</strong></p><p>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.</p><p>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.</p><p><strong>Key Responsibilities</strong></p><p><strong>Participant Screening &amp; Assessment</strong></p><ul><li>Review subject medical histories and conduct pre-screening interviews to assess eligibility for specific clinical trials</li><li>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</li><li>Calculate and apply rating scale results to determine protocol eligibility under the supervision of the Principal Investigator</li><li>Conduct telephone pre-screens and eligibility interviews as needed</li></ul><p><strong>Data Integrity &amp; Documentation</strong></p><ul><li>Maintain accurate, complete, and timely source documentation in accordance with ALCOA-C standards</li><li>Complete all sponsor- and monitor-assigned queries within required timeframes</li><li>Actively work to maintain consistency in rating performance over time for individual subjects to prevent rater drift</li><li>Maintain strict confidentiality of participant and company information in compliance with HIPAA guidelines</li></ul><p><strong>Participant Safety &amp; Communication</strong></p><ul><li>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</li><li>Provide appropriate community resource referrals to participants, caregivers, and family members as needed</li><li>Facilitate timely, professional communication with participants, study staff, Sponsors, CROs, Monitors, Auditors, and central rating organizations</li><li>Articulate rating concerns or issues to the CRO, Sponsor, Principal Investigator, and study team</li></ul><p><strong>Team Leadership &amp; Training</strong></p><ul><li>Serve as study lead across a minimum of four concurrent studies</li><li>Provide weekly schedule oversight for a minimum of two study coordinators</li><li>Complete all Sponsor-assigned rater training and maintain certification and re-certification per protocol requirements</li><li>Attend Sponsor meetings, Monitor visits, webinars, and company training programs</li><li>Perform additional duties as assigned</li></ul><p><strong>Ideal Candidate Profile</strong></p><p>Someone who:</p><ul><li>Understands how rigorous, consistent ratings directly impact clinical trial outcomes</li><li>Notices when a participant interaction is off-protocol and proactively corrects course</li><li>Is comfortable working across research, clinical, and sponsor-facing teams without close supervision</li><li>Brings genuine empathy and professionalism when working with participants of varying cognitive abilities</li><li>Takes ownership of rater certification, re-certification, and quality standards</li></ul>",
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      "datePosted": "2026-05-21T17:55:06-05:00",
      "description": "<p>Description</p><p> </p><p><em>Job Description  |  Full-Time |  On-Site</em></p><p><strong>Position Summary</strong></p><p>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.</p><p>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.</p><p><strong>Key Responsibilities</strong></p><p><strong>Participant Screening & Assessment</strong></p><ul><li>Review subject medical histories and conduct pre-screening interviews to assess eligibility for specific clinical trials</li><li>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</li><li>Calculate and apply rating scale results to determine protocol eligibility under the supervision of the Principal Investigator</li><li>Conduct telephone pre-screens and eligibility interviews as needed</li></ul><p><strong>Data Integrity & Documentation</strong></p><ul><li>Maintain accurate, complete, and timely source documentation in accordance with ALCOA-C standards</li><li>Complete all sponsor- and monitor-assigned queries within required timeframes</li><li>Actively work to maintain consistency in rating performance over time for individual subjects to prevent rater drift</li><li>Maintain strict confidentiality of participant and company information in compliance with HIPAA guidelines</li></ul><p><strong>Participant Safety & Communication</strong></p><ul><li>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</li><li>Provide appropriate community resource referrals to participants, caregivers, and family members as needed</li><li>Facilitate timely, professional communication with participants, study staff, Sponsors, CROs, Monitors, Auditors, and central rating organizations</li><li>Articulate rating concerns or issues to the CRO, Sponsor, Principal Investigator, and study team</li></ul><p><strong>Team Leadership & Training</strong></p><ul><li>Serve as study lead across a minimum of four concurrent studies</li><li>Provide weekly schedule oversight for a minimum of two study coordinators</li><li>Complete all Sponsor-assigned rater training and maintain certification and re-certification per protocol requirements</li><li>Attend Sponsor meetings, Monitor visits, webinars, and company training programs</li><li>Perform additional duties as assigned</li></ul><p><strong>Ideal Candidate Profile</strong></p><p>Someone who:</p><ul><li>Understands how rigorous, consistent ratings directly impact clinical trial outcomes</li><li>Notices when a participant interaction is off-protocol and proactively corrects course</li><li>Is comfortable working across research, clinical, and sponsor-facing teams without close supervision</li><li>Brings genuine empathy and professionalism when working with participants of varying cognitive abilities</li><li>Takes ownership of rater certification, re-certification, and quality standards</li></ul><p>Requirements</p><p> <strong>Required Qualifications</strong></p><ul><li>Minimum Bachelor's degree (B.A. or B.S.) in Psychology, Neuroscience, or a closely related field</li><li>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</li><li>Solid working knowledge of clinical research protocols, FDA regulations, GCP, and ICH guidelines</li><li>Experience conducting cognitive and clinical assessments with adult and/or geriatric populations</li><li>Strong documentation skills with demonstrated attention to detail</li><li>Proficiency with Microsoft Office, EHR platforms, email, and web-based applications; 40+ WPM typing</li><li>Strong written and verbal communication skills and ability to work cross-functionally</li></ul><p><strong>Preferred Qualifications</strong></p><ul><li>Master's degree in Psychology, Neuroscience, or a related field; Certified Psychometrist designation is a plus</li><li>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</li><li>Bilingual proficiency in English and Spanish</li><li>BLS certification</li><li>Experience supervising or mentoring junior staff in a clinical research environment</li></ul>",
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