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Clinical Rater

Proclinical Brookline 14.10.2026 Bewerbung einreichen
Unternehmen
Proclinical
Ort
Brookline
Datum
14.10.2026
Referenznummer
367400

Clinical Rater Opportunity in Brookline, MA

Are you a doctoral-level clinician with extensive experience administering psychiatric and neurological rating scales in clinical research settings? This contract role focuses on clinical rating-scale administration within the neurology and biotechnology space, seeking a professional with specific expertise in administering clinical scales.

Primary Responsibilities

  • Administer clinical rating scales as part of clinical trials, ensuring accuracy and adherence to protocols.
  • Conduct assessments using tools such as the Brief Psychiatric Rating Scale (BPRS), Clinician-Administered Dissociative States Scale (CADSS), Clinical Global Impression Scales (CGI-I and CGI-S), and others as required.
  • Maintain detailed and accurate documentation of all assessments.
  • Collaborate with clinical teams to ensure data integrity and compliance with trial requirements.
  • Stay updated on certification requirements and maintain proficiency in administering scales.

Skills and Requirements

Doctoral-level clinician (PhD, PsyD, or DO) with experience in clinical rating scales. Proficiency in administering the following scales with recent experience (within the past 6 months to 2 years) is required:

  • BPRS: Minimum 20 administrations
  • CADSS: Minimum 10 administrations
  • CGI-I and CGI-S: Minimum 25 administrations each
  • C-SSRS: Minimum 20 administrations and Columbia Lighthouse Project certification
  • MADRS: Minimum 25 administrations
  • MGH-ATRQ: Minimum 25 administrations
  • MINI: Minimum 25 administrations
  • MOAA-S: Minimum 10 administrations
  • YMRS: Minimum 20 administrations
  • GAD-7: Minimum 20 administrations
  • QIDS-SR: Minimum 20 administrations
  • DSST: Minimum 10 administrations

Familiarity with additional scales such as SETS-P, PCRS, BPIC-SS, and PWC-20 is preferred. Candidates must demonstrate strong attention to detail and the ability to follow clinical trial protocols, along with excellent communication and interpersonal skills.

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