PURPOSEResponsible for administering clinical study assessments on a neurological study (EDSS rating). 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 neurological 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 PIEDUCATION AND EXPERIENCE• Medical degree-PhD, MD or DO, will consider PA or NP with extensive rating experience• Minimum two years of clinical experience and research experience with neurological population• Minimum two years of EDSS rater experience supporting clinical trials• Competency in rating scales as required by studies. Experience in specific scales will be assessed as needed for specific projects. Raters will undergo study rater training as required for each project. Compliance with all in-study rater training obligations and certification processes through trial duration.Required Scales with Experience Rating:--EDSS certification through NeuroStatus platform.--Examining Investigator/rater should have prior 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#HCPN #Onsite #LI-CES and #LI-DNPIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. ability to operate and provide certain services to customers and partners necessitates IQVIA and its employees meet specific requirements regarding COVID-19 vaccination status. potential base pay range for this role is The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.IQVIA is a world leader in using data, technology, advanced analytics, and expertise to help customers drive healthcare – and human health – forward. Together with the companies we serve, we are enabling a more modern, more effective and more efficient healthcare system, and creating breakthrough solutions that transform business and patient outcomes.To get there, it takes diverse skills and a curiosity to explore new possibilities. No matter your role, everyone at IQVIA contributes to our shared goal of improving human health. Thank you for your interest in growing your career with us.EEO Minorities/Females/Protected Veterans/Disabled