Job Posting Title Clinical Trial Psych Rater - German Speaking

IQVIA; Berlin; Remote; USD 6,696 - 10,044; Part time

Job summary

IQVIA is seeking a Clinical Specialist to support German-speaking clinical trial assessments. The role involves reviewing scales, guiding raters on methodology and scoring, and contributing to rater calibration and documentation.

This part-time, remote position requires English fluency and native German. Ideal candidates hold a Master’s degree in psychology or related field, at least 3 years in psychiatric assessments and in clinical research, plus familiarity with BEHAVE-AD and CNS trials.

Qualifications

• Master’s degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing, Social Work, or equivalent; MD/DO/PhD preferred.
• At least 3 years administering psychiatric assessments, rating scales, or structured interviews (e.g., BEHAVE-AD, E-BEHAVE-AD).
• At least 3 years of clinical experience with psychiatric populations.
• At least 3 years administering scales in clinical research trials (excluding grad/doctoral work).
• Experience in CNS trials preferred.

Responsibilities

• Participate in orientation, training, and calibration activities.
• Review case data and prepare for rater discussions.
• Conduct live feedback with raters on assessment methodology and scoring.
• Complete tasks and rater interactions according to schedule.
• Submit documentation accurately and on time.

Skills

Interpersonal

Organizational

Time management

Communication

Education

Master’s degree in psychology or related field

MD/DO/PhD preferred

Tools

Windows

Microsoft Office

Job description

## Job Posting Title Clinical Trial Psych Rater - German SpeakingApplylocations: Berlin, Germany: Gilbert, AZ, United States of America: San Francisco, CA, United States of America: Austin, TX, United States of America: Moreno Valley, CA, United States of Americatime type: Part timeposted on: Posted Todayjob requisition id: R1559917# **Clinical Trial Psych Rater -** **German** **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** **BEHAVE,-AD, E-BEHAVE-AD, BEHAVE-AD-FW, NPIC, ADAS-Cog; CGI-S, C-SSRS****)** + 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 German.**#LI-DNP #LI-Remote #LI-HCPN