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Clinical Trial Psych Sdic & Ymrs Rater - Remote - Marathi, Malayalam, Or Bengali Languages As Well As English

3+ years
Not Disclosed
10 Dec. 26, 2024
Job Description
Job Type: Part Time Education: MA/MS 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

Job Title: Clinical Specialist Consultant

Location: IQVIA Laboratories


About IQVIA: IQVIA is a leading global provider of clinical research services, healthcare intelligence, and commercial insights for the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments, ultimately improving patient outcomes and population health.


Role Summary: As a Clinical Specialist Consultant, you will review scales administered by raters in clinical trials to ensure that assessments are being conducted in a standardized manner. You will ensure the reliability of the data by evaluating assessment quality, interacting with raters to provide guidance on assessment methodology and scoring, and conducting functional assessments of rater performance.


Key Responsibilities:

  1. Rater Interaction & Assessment:

    • Evaluate case data and engage in discussions with raters about assessment methodologies and scale items.
    • Conduct live interactions with raters to review the quality of assessments and provide necessary feedback and guidance.
  2. Training & Calibration:

    • Participate in all orientation, training, and calibration activities as required for trials.
    • Prepare for discussions with raters by ensuring relevant issues and scale items are clearly understood.
  3. Documentation & Compliance:

    • Ensure all documentation related to assigned tasks is completed and submitted in a timely manner.
    • Maintain accurate records of rater performance, interactions, and any issues encountered during assessments.
  4. Support for Clinical Research:

    • Assist in preparing and disseminating communications related to the clinical trials and assessments.
    • Support the ongoing evaluation and improvement of assessment techniques and rater performance.

Qualifications:

  • Education: Master’s degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing, Social Work, or equivalent.
  • Experience:
    • Minimum of 3 years of experience administering psychiatric assessments, rating scales, and/or structured clinical interviews.
    • At least 3 years of clinical experience with related psychiatric populations.
    • A minimum of 3 years of experience administering scales in clinical research trials (excluding graduate/doctoral research work).
    • Experience in central nervous system (CNS) trials is preferred.
  • Skills:
    • Strong interpersonal skills and the ability to interact professionally with all levels of personnel and clients.
    • Excellent organization, attention to detail, time management, and problem-solving abilities.
    • Proficient with Windows and Microsoft Office applications.

Language Requirements:

  • Current openings require fluency in English, with a preference for native speakers of the language needed for the trial.

What We Offer:

  • Opportunities to work in a leading clinical research environment, contributing to important studies in healthcare.
  • Professional development in clinical research, assessment, and clinical trial operations.

Apply Now and join IQVIA to help drive innovation in clinical trials and make a meaningful impact on patient care.


IQVIA is committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. For more information about our open positions, visit IQVIA Careers.