Clinical Specialist/Rater

IQVIA, Inc.; Reading; Remote; GBP 30,000 - 45,000; Part time

Job summary

A leading global provider of clinical research services is seeking a Clinical Specialist Consultant to ensure standardized assessments in clinical trials. This remote role involves evaluating assessment quality and engaging with raters. Ideal candidates will have a Master's degree and significant experience in psychiatric assessments.

Qualifications

• Minimum 3 years' experience administering psychiatric assessments.
• Experience with administering scales in clinical research trials.

Responsibilities

• Evaluate case data and prepare for discussions with raters.
• Ensure timely submission of all related documentation.

Skills

Interpersonal Skills

Organization

Attention to Detail

Time Management

Problem Solving

Education

Master's degree in Psychology

MD, DO, or PhD

Tools

Windows

Microsoft Office

Job description

Clinical Specialist Consultant

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 assessments are conducted in a standardized manner, ensuring data reliability. Responsibilities include evaluating assessment quality, engaging in live interactions with raters to discuss methodology and scoring, and providing guidance as needed. Additional tasks may include functional assessments of rater performance (e.g., mock interviews) and assisting in preparing and disseminating communications.

Required Experience, Knowledge, Skills:

• 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' experience administering psychiatric assessments, rating scales, and structured clinical interviews.
• Minimum of 3 years of clinical experience with related psychiatric populations.
• At least 3 years of experience with administering scales in clinical research trials (excluding graduate/doctoral research).
• Experience in CNS trials is preferred.
• Strong interpersonal skills to interact professionally with all levels of personnel and clients.
• Excellent organization, attention to detail, time management, and problem-solving skills.
• Proficiency in Windows and Microsoft Office applications.

Tasks/Responsibilities:

• Participate in orientation, training, and calibration activities as required.
• Evaluate case data and prepare for discussions with raters, including discussing relevant issues and scale items, and having necessary documents ready.
• Complete assigned tasks and rater interactions timely.
• Ensure timely submission of all related documentation.

Current openings require fluency in English and native proficiency in the language needed for the trial.

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 improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com