Clinical Specialist Consultant - Swedish Speaking
Location: Remote/virtual
Hours: Estimated 10-16h/month
Role: Clinical Specialist
Job Description:
The Clinical Specialist reviews scales administered by raters in a clinical trial to ensure that assessments are being conducted in a standardized manner to ensure data reliability. The quality of assessments is evaluated, and live interaction with raters is conducted to discuss assessment methodology, scoring technique, and to provide guidance, as necessary. Other Clinical Specialist responsibilities may include, but are not limited to, functional assessments of rater performance (e.g., mock interview) and assistance in preparing and disseminating communications.
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. Specifically, Primary: SIGH-A, SCID, MADRS/SIGMA, HDRS-17, ISI and PHQ-9 Secondary: CSSRS, CGI-S/I
• Minimum of 3 years clinical experience with related psychiatric populations.
• Minimum of 3 years' experience with administering scales in clinical research trials (not including graduate/doctoral research work).
• Experience in central nervous system (CNS) trials preferred.
• Strong interpersonal skills with ability to interact with all levels of personnel and clientele in a professional manner.
• Excellent organization, attention to detail, time management and problem-solving skills.
• Computer proficiency with Windows and Microsoft Office system and applications.
Tasks/Responsibilities:
• Participate in all orientation, training and calibration activities as required.
• Evaluate case data and appropriately prepare for discussions with raters (e.g., prepared to 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 assigned tasks.
*Current openings require fluency in English and a native speaker in the language needed for the trial.
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IQVIA 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 https://jobs.iqvia.com
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IQVIA (NYSE:IQV) is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. IQVIA creates intelligent connections across all aspects of healthcare through its analytics, transformative technology, big data resources and extensive domain expertise. IQVIA Connected Intelligence™ delivers powerful insights with speed and agility — enabling customers to accelerate the clinical development and commercialization of innovative medical treatments that improve healthcare outcomes for patients. With approximately 70,000 employees, IQVIA conducts operations in more than 100 countries. To learn more, visit www.iqvia.com.
