Clinical Trial Rater - Chinese speaker at IQVIA

Beijing, Beijing, China

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Not SpecifiedCompensation

Mid-level (3 to 4 years)Experience Level

Part TimeJob Type

UnknownVisa

Healthcare, Clinical ResearchIndustries

Requirements

Minimum of a Master’s degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing, Social Work, or equivalent. MD, DO, or PhD preferred
At least 3 years of experience administering psychiatric assessments, rating scales, and structured clinical interviews
Experience with EQ-5D-5L
Minimum of 3 years working with psychiatric populations
At least 3 years of experience administering scales in clinical research trials (excluding graduate/doctoral research work)
Preferred: Experience in central nervous system (CNS) trials
Strong interpersonal skills, excellent organization, attention to detail, time management, and problem-solving abilities
Proficiency with Windows and Microsoft Office applications
Fluent Chinese language skills

Responsibilities

Reviewing scales administered by raters to ensure standardized assessments
Conducting patient assessment and administer rating scales
Evaluating the quality of assessments and providing live interaction with raters to discuss methodologies, scoring techniques, and offer guidance
Conducting functional assessments of rater performance (e.g., mock interviews)
Assisting in preparing and disseminating communications
Participate in all orientation, training, and calibration activities
Evaluate case data and prepare for discussions with raters, ensuring relevant issues and scale items are addressed
Complete rater interactions and assigned tasks as scheduled
Ensure timely submission of all documentation related to assigned tasks

Skills

Key technologies and capabilities for this role

psychiatric assessmentsrating scalesstructured clinical interviewsEQ-5D-5LMicrosoft OfficeWindowsChinese

Questions & Answers

Common questions about this position

Is this position remote?

Yes, the position is remote/virtual.

How many hours per week is this role?

The role is part-time with estimated 2-5 hours per week.

What education and experience are required?

A minimum of a Master’s degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing, Social Work, or equivalent is required, along with at least 3 years of experience administering psychiatric assessments, rating scales, structured clinical interviews, working with psychiatric populations, and administering scales in clinical research trials (excluding graduate/doctoral research). MD, DO, or PhD is preferred, as is experience in CNS trials and with EQ-5D-5L.

What skills are needed for this role?

Strong interpersonal skills, excellent organization, attention to detail, time management, problem-solving abilities, proficiency with Windows and Microsoft Office, and fluent Chinese language skills are required.

What makes a strong candidate for this Clinical Trial Rater position?

Candidates with a Master’s degree or higher in a relevant field, 3+ years of direct experience in psychiatric assessments and clinical research trials with psychiatric populations, experience with EQ-5D-5L and CNS trials, plus strong organizational skills and fluent Chinese will stand out.

IQVIA

Advanced analytics and clinical research services

About IQVIA

IQVIA provides advanced analytics, technology solutions, and clinical research services specifically for the life sciences industry. Their services utilize extensive data resources and technology to create connections within healthcare, allowing clients to gain insights that help speed up the development and marketing of new medical treatments. This process is facilitated by their IQVIA Connected Intelligence™ system, which offers quick and flexible insights. IQVIA stands out from competitors by focusing on patient privacy, employing various technologies to protect individual data. The company's goal is to enhance healthcare outcomes by supporting biotech, pharmaceutical, and medical device companies, as well as researchers and government agencies, in understanding diseases and advancing medical science.

Durham, North CarolinaHeadquarters

1998Year Founded

$3,526MTotal Funding

POST_IPO_EQUITYCompany Stage

Cybersecurity, Biotechnology, HealthcareIndustries

10,001+Employees

Risks

Rapid advancement of cancer vaccines may disrupt traditional clinical research models.

Proliferation of disparate technological solutions causes technology overload in clinical trials.

Generative AI technologies face challenges in adoption due to data privacy concerns.

Differentiation

IQVIA leverages advanced analytics and big data for life sciences solutions.

The company offers privacy-enhancing technologies to protect individual patient data.

IQVIA's AI Assistant provides rapid, actionable insights for healthcare and life sciences.

Upsides

Increased adoption of decentralized clinical trials enhances patient-centric study designs.

AI-driven drug discovery accelerates identification of potential drug candidates.

Expansion of telemedicine facilitates remote patient monitoring and data collection.

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