PURPOSE

Responsible for administering clinical study assessments on a study. Observes the study participant’s

symptoms and documents observations appropriately via psychiatric rating scales in accordance with

study-specific requirements. Follows individual study participants through the study lifecycle and

maintains documentation of observations for reporting purposes.

RESPONSIBILITIES

• Administer clinical rating scales to support the diagnosis and assessment of symptom severity of subjects participating in CNS clinical studies.
• Attends, completes, and qualifies for study-specific rater training and certification for trials on which they rate.
• Measures the severity of symptoms of study participants
• Continuously observe the study participants using approved assessments throughout study
• Reports to and works under the guidance of the principal investigator and / or sub-investigator for the study site where the study participant is seen
• Assist team in management and assessment of adverse events
• Support PI / Sub-I and study coordinators with assessments, data clarification, and data query completion
• Serve as Sub-I where applicable under the delegation of the PI

EDUCATION AND EXPERIENCE

25 assessments in the last year preferable

ADDITIONAL ATTRIBUTES

LI-DNP

LI-HCPN

LI-CES

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at