Clinical Trial Psych Rater

Há 2 dias

Região Geográfica Imediata de Criciúma, Brasil IQVIA Tempo inteiro

Overview

Clinical Trial Psych Rater - Portuguese Speaking role at IQVIA. Remote/virtual location with approximately 10-16 hours per month. Role: Clinical Specialist with focus on ensuring standardized administration and reliability of assessments in clinical trials.

Responsibilities
  • Participate in all orientation, training and calibration activities as required.
  • Evaluate case data and prepare for discussions with raters, including relevant issues and scale items, with necessary documents available.
  • Complete rater interactions and assigned tasks as scheduled.
  • Ensure timely submission of all documentation associated with assigned tasks.
  • Current openings require fluency in English and native speaker proficiency in the language needed for the trial.
Required Experience, Knowledge, Skills
  • Minimum of a master’s degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing or Social Work, or equivalent. MD, DO or PhD preferred.
  • Minimum of 3 years’ experience administering psychiatric assessments, ratings scales and/or structured clinical interviews (e.g., MADRS/SIGMA; CGI-S, C-SSRS, HDRS-17, ISI, PHQ-9).
  • Minimum of 3 years clinical experience with related psychiatric populations.
  • Minimum of 3 years experience administering scales in clinical research trials (not including graduate/doctoral research work).
  • Experience in central nervous system (CNS) trials preferred.
  • Strong interpersonal skills to interact professionally with all levels of personnel and clients.
  • Excellent organization, attention to detail, time management and problem-solving skills.
  • Computer proficiency with Windows and Microsoft Office applications.
Tasks/Responsibilities
  • Participate in orientation, training and calibration activities as required.
  • Evaluate case data and prepare for discussions with raters (e.g., discuss relevant issues and scale items, and have necessary documents available).
  • Complete rater interactions and assigned tasks as scheduled.
  • Responsible for timely submission of all documentation associated with tasks.
Additional Information

IQVIA is a leading global provider of clinical research services and healthcare insights. Learn more at IQVIA values diversity, inclusion, and belonging in the workplace.

Seniority level
  • Not Applicable
Employment type
  • Part-time
Job function
  • Research, Analyst, and Information Technology
Industries
  • Pharmaceutical Manufacturing
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