[Skip to main content](#main-content) [OpenNash Jobs](https://jobs.opennash.com/) [Hiring report](/reports/hiring/) · [All IQVIA jobs](https://jobs.opennash.com/companies/iqvia/) · [Search jobs](/search/) IQVIA · Multiple locations # Clinical Trial Psych Rater - Latvian Speaking Multiple locations Healthcare & Clinical Listed on IQVIA’s official careers site. Listed as of October 17, 2026. Check that it is still open and apply there. [Apply on IQVIA’s careers site →](https://iqvia.wd1.myworkdayjobs.com/IQVIA/job/Riga-Latvia/Clinical-Trial-Psych-Rater---Latvian-Speaking_R1558279) [OpenNash Jobs](https://jobs.opennash.com/) / [IQVIA](https://jobs.opennash.com/companies/iqvia/) / Clinical Trial Psych Rater - Latvian Speaking ## Job description ### Clinical Trial Psych Rater - Latvian Speaking Location Remote/Virtual Hours: Estimated 10–16 hours per month Role: Clinical Specialist About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare forward. We partner with the world’s leading pharmaceutical, biotechnology, and medical device companies to improve patient outcomes and accelerate innovation. Our team combines deep scientific expertise with cutting-edge technology to deliver high-quality data and insights that shape the future of clinical trials. ### Position Overview The Clinical Specialist plays a key role in ensuring the integrity and reliability of clinical trial data. This position involves reviewing scales administered by raters to confirm standardized assessment practices. Responsibilities include evaluating assessment quality, engaging in live discussions with raters to provide guidance on methodology and scoring techniques, and supporting rater performance through functional assessments (e.g., mock interviews). Additional tasks may include assisting with communication materials and documentation. ### Key Responsibilities Participate in all required orientation, training, and calibration activities. Review case data and prepare for rater discussions, ensuring all relevant documents and scale items are available. Conduct live interactions with raters to provide feedback and guidance on assessment methodology and scoring. Complete assigned tasks and rater interactions according to schedule. Submit all required documentation accurately and on time. ### Required Qualifications Education: Master’s degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing, or Social Work (or equivalent). MD, DO, or PhD preferred. ### Experience Minimum 3 years administering psychiatric assessments, rating scales, and/or structured clinical interviews (specifically EQ-5D-5L (Interviewer administered and Proxy 1 version) & mRS). Minimum 3 years of clinical experience with psychiatric populations. Minimum 3 years administering scales in clinical research trials (excluding graduate/doctoral research). Experience in CNS trials preferred. ### Skills Strong interpersonal and communication skills for professional interaction at all levels. Excellent organizational skills, attention to detail, time management, and problem-solving ability. Proficiency with Windows and Microsoft Office applications. Language Requirement Current openings require fluency in English and native-level proficiency in Latvian. #LI-DNP #LI-Remote #LI-HCPN 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](https://jobs.iqvia.com) IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. ## At a glance - Posted by the employer: Not stated - First seen by OpenNash: Oct 10, 2026 - Last checked: Oct 17, 2026 - Listed for: 7 days - Location: Multiple locations[Apply on IQVIA’s careers site →](https://iqvia.wd1.myworkdayjobs.com/IQVIA/job/Riga-Latvia/Clinical-Trial-Psych-Rater---Latvian-Speaking_R1558279) ## More jobs at IQVIA ### [(Senior) Clinical Research Associate (CRA)](https://jobs.opennash.com/companies/iqvia/jobs/18369455a0bcaec6dd79/) ### [(Senior) Clinical Research Associate - Sponsor dedicated - Türkiye](https://jobs.opennash.com/companies/iqvia/jobs/0e5a17bac181bde47316/) ### [Associate Director, Client Services - IQVIA Medical Communications](https://jobs.opennash.com/companies/iqvia/jobs/741a75e5f7714284464f/) ### [Associate Solution and Delivery Lead, Healthcare & Pharma](https://jobs.opennash.com/companies/iqvia/jobs/72442d5379da5a50017f/) ### [Associé(e) de recherche clinique (ARC) principal(e) / Senior Clinical Research Associate, Sponsor Dedicated](https://jobs.opennash.com/companies/iqvia/jobs/82bb761af95fb7f1ffb4/) ## Similar jobs at other companies ### [Associate Director Clinical Trial Technology, IRT](https://jobs.opennash.com/companies/csl/jobs/145bba0747b03bd41a44/) CSL ### [Senior Clinical Trial Case Manager](https://jobs.opennash.com/companies/csl/jobs/a181a37634b0c8cce5f7/) CSL ### [Head of Clinical Trial Start Up](https://jobs.opennash.com/companies/biogen-idec/jobs/51b3987b65deca4d2122/) Biogen ### [Clinical Trial Assistant - Student Placement](https://jobs.opennash.com/companies/johnson-johnson/jobs/89f90a65eda7769652ad/) Johnson & Johnson ### [Clinical Trial Physician, Cell Therapy, Medical Evidence Generation](https://jobs.opennash.com/companies/bristol-myers-squibb/jobs/f884d514caabc0debedf/) Bristol Myers Squibb OpenNash lists jobs from employers’ own careers sites and does not handle applications. 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