Neuro Psychiatric Rater - United Kingdom/Travel in UK

Social network you want to login/join with: Neuro Psychiatric Rater – United Kingdom/Travel in UK, Newport col-narrow-left Client: IQVIA Location: Newport, United Kingdom Job Category: Other – EU work permit required: Yes col-narrow-right Job Reference: 07287751e079 Job Views: 4 Posted: 02.06.2025 Expiry Date: 17.07.2025 col-wide Job Description: 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 ofsubjects participating in CNS clinical studies. • Attends, completes, and qualifies for study-specific rater training and certification for trials onwhich 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 forthe 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 querycompletion• Serve as Sub-I where applicable under the delegation of the PI EDUCATION AND EXPERIENCE • Medical Degree-Board certified psychiatrist PhD, MD or DO • Minimum two years of clinical experience and research experience with neuropsychiatricpopulation • Minimum two years of neuro psychiatric rater experience preferably, supporting clinical trials o > 25 assessments in the last year preferable • Competency in rating scales as required by studies. Experience in specific scales will beassessed as needed for specific projects. Raters will undergo study rater training as required foreach project. Compliance with all in-study rater training obligations and certification processes through trial duration. 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 #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 #J-18808-Ljbffr