Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Clinical Trial Psych Rater - Gujarati Speaking

Iqvia
IQVIA
3+ years
Not Disclosed
10 Jan. 1, 2026
Job Description
Job Type: Part Time Remote Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Clinical Trial Psych Rater – Gujarati Speaking (Remote / Home-Based, India)

Category: Clinical Research / CNS & Psychiatric Trials
Locations: Remote / Home-Based (Mumbai, Ahmedabad, Surat, and other Indian locations)
Employment Type: Part-Time / Contract
Estimated Hours: 10–16 hours per month
Role Level: Clinical Specialist Consultant


About IQVIA

IQVIA is a global leader in clinical research, analytics, and technology solutions, partnering with top pharmaceutical, biotech, and medical device companies. We deliver high-quality data, insights, and clinical trial support that accelerate innovation and improve patient outcomes worldwide.

Learn more: https://jobs.iqvia.com


Position Overview

The Clinical Trial Psych Rater / Clinical Specialist Consultant ensures accuracy and consistency of psychiatric assessments in CNS and psychiatric clinical trials. You will review rating scales, evaluate assessment quality, and provide real-time guidance to raters. This role also involves training, calibration sessions, mock interviews, and maintaining compliance with study protocols.

Fluency in Gujarati and English is required.


Key Responsibilities

  • Attend orientation, training, and calibration sessions as required.

  • Review case data and prepare documentation for rater discussions.

  • Conduct scheduled rater interactions and provide guidance on scoring techniques and methodology.

  • Complete tasks and submit all documentation accurately and on time.

  • Support consistency and compliance in CNS/psychiatric clinical trials.

  • Participate in mock interviews and support communication efforts across trial teams.


Qualifications & Experience

  • Education: Master’s degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing, or Social Work (or equivalent). MD, DO, or PhD preferred.

  • Experience:

    • 3+ years administering psychiatric assessments, rating scales, and structured clinical interviews (including EQ-5D-5L Interviewer-administered / Proxy 1 version & smRS).

    • 3+ years clinical experience with psychiatric populations.

    • 3+ years administering scales in clinical research trials (excluding graduate/doctoral work).

    • CNS trial experience is a plus.

  • Skills:

    • Strong interpersonal and communication skills for professional interaction at all levels.

    • Excellent organizational skills, attention to detail, and time management.

    • Proficiency with Windows and Microsoft Office applications.

  • Language Requirement: Fluent in English and native-level proficiency in Gujarati.


Why Work With IQVIA

  • Flexible, remote part-time work schedule.

  • Contribute to global psychiatric clinical research.

  • Collaborate with a science-driven, diverse team committed to advancing patient care.

  • Gain experience in global clinical trial methodology and CNS trial standards.