20 beste Stellen als clinical trial leader in basel bs – aktuell auf Personalsuche

Clinical Independent Rater for Clinical Trial - Turkish Speaking
IQVIA —Basel, BS
- Teilzeit
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- Doktorat
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- Forschungserfahrung
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9 Tage
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Clinical Independent Rater for Clinical Trial - Turkish Speaking

IQVIA -
Basel, BS

Jetzt bewerben

Details zur Stelle

Teilzeit
vor 9 Tagen

Leistungen

Homeoffice-Möglichkeit

Qualifikationen

Doktorat
Englisch
Forschungserfahrung
Windows
Microsoft Office
Klinische Erfahrung
Master
Organisationstalent
Kommunikationsfähigkeit
Zeitmanagement

Vollständige Stellenbeschreibung

Basel, Switzerland | Part time | Home-based | R1565310

Clinical Independent Rater - Turkish Speaking

Location: Remote/Virtual
Hours: Estimated 10–16 hours per month
Role: Clinical Independent Rater for Clinical Trials

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 CIR 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 assessment materials are available.
Conduct patient interviews and clinical assessments with study participants.
Administer, score, and interpret clinical rating scales and structured interviews.
Provide feedback and guidance to raters on assessment methodology, interview techniques, and scoring accuracy through live interactions.
Complete assigned assessments, rater interactions, and related activities according to study timelines and schedules.
Work directly with study participants while maintaining protocol compliance and data quality standards.
Submit all required documentation, reports, and assessment records accurately and within required timelines.

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 MINI and MADRS).
- 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 Turkish.

#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

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.

Where you'll work

Home-based

You’ll work remotely, with the flexibility to do your best work from home. Supported by collaborative tools and a global team, you’ll stay connected while enjoying the autonomy and balance that comes with a fully remote role.

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

Jetzt bewerben

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Ich möchte aktuelle Job-E-Mails für Stellen als clinical trial leader in basel bs erhalten

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Clinical Independent Rater - Turkish Speaking

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