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Clinical Trial Neuro/Psych Rater

2 months ago

Savannah, Georgia, United States IQVIA Full time
Job Summary

We are seeking a highly skilled Clinical Trial Neuro/Psych Rater to join our team at IQVIA. As a Clinical Trial Neuro/Psych Rater, you will be responsible for administering clinical study assessments, observing study participants, and documenting observations accurately.

Key Responsibilities
  • Administer clinical rating scales to support the diagnosis and assessment of symptom severity of subjects participating in CNS and neuro/psych clinical studies.
  • Attend, complete, and qualify for study-specific rater training and certification for trials on which they rate.
  • Measure the severity of symptoms of study participants.
  • Continuously observe the study participants using approved assessments throughout the study.
  • Report to and work under the guidance of the principal investigator and/or sub-investigator for the study site where the study participant is seen.
  • Assist the team in management and assessment of adverse events.
  • Support the principal investigator/sub-investigator and study coordinators with assessments, data clarification, and data query completion.
  • Serve as a sub-investigator where applicable under the delegation of the principal investigator.
Requirements
  • A medical degree (PhD, MD, or DO) or a Physician Assistant (PA) or Nurse Practitioner (NP) with extensive rating experience.
  • Minimum two years of clinical experience and research experience with a neuropsychiatric population.
  • Minimum two years of rater experience supporting clinical trials, with more than 25 assessments in the last year preferred.
  • Competency in rating scales as required by studies, with experience in specific scales assessed as needed for specific projects.
Preferred Qualifications
  • EDSS certification through the NeuroStatus platform.
  • Experience conducting the EDSS assessment and other efficacy assessments (T25FWT and 9HPT).
Additional Attributes
  • Functional knowledge of ICH/GCP guidelines.
  • Functional knowledge of HIPAA and its application to clinical research.
  • Excellent oral and written communication skills.
  • Ability to function independently.