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Clinical Trial Psych Rater - Odiya Speaking

Iqvia
IQVIA
1 years
Not Disclosed
Remote
1 May 6, 2026
Job Description
Job Type: Part Time Education: Minimum: Master’s degree (MA/MS) in Medicine, Neurology, Psychology, or related field. Preferred: MD, DO, or PhD. 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 Specialist / Stroke Rater – Odiya Speaking

Location: Remote
Job Type: Part-Time / Flexible Hours
Estimated Hours: 2–12 Hours per Month
Experience Required: Minimum 1 Year of Clinical Experience in Stroke Care or Clinical Trials
Language Requirement: Fluent in Odiya


About the Role

We are seeking a detail-oriented and experienced Clinical Specialist / Stroke Rater (Odiya Speaking) to support ongoing stroke-related clinical trials in a remote capacity. The ideal candidate will play a critical role in ensuring the accuracy, consistency, and quality of clinical assessments conducted across trial participants and research teams.

This position is ideal for healthcare professionals with prior exposure to stroke patient evaluation, clinical research protocols, and standardized stroke rating scales. Candidates must possess strong analytical, communication, and assessment skills while maintaining strict adherence to clinical trial standards and compliance requirements.


Key Responsibilities

  • Administer standardized stroke assessment scales, including Modified Rankin Scale (mRS) and EQ-5D-5L, for clinical trial participants.
  • Review and evaluate assessments completed by other stroke raters to ensure protocol accuracy and inter-rater consistency.
  • Conduct live review sessions and provide professional feedback on scoring methodologies and assessment techniques.
  • Participate in onboarding, certification, calibration, and ongoing training sessions to maintain rating quality standards.
  • Analyze case documentation and patient data prior to scheduled rater discussions and evaluations.
  • Complete all assigned reviews, documentation, and compliance-related activities within project timelines.
  • Support mock interviews, quality assurance checks, and performance evaluations for clinical raters when required.
  • Maintain confidentiality, regulatory compliance, and high-quality clinical documentation standards throughout all trial activities.

Required Qualifications

Educational Qualifications

Minimum Requirement:

  • Master’s Degree (MA/MS) in:
    • Medicine
    • Neurology
    • Psychology
    • Life Sciences
    • Or a related healthcare discipline

Preferred Qualification:

  • MD, DO, or PhD in a relevant clinical or medical field