Instagram
youtube
Facebook

Clinical Trial Psych Sdic & Ymrs Rater - Remote - Oriya, Panjabi, (Eastern), Kannada, Malayalam, Assamese 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, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. Our mission is to accelerate the development and commercialization of innovative medical treatments to improve patient outcomes and population health.


Role Overview: As a Clinical Specialist Consultant, you will review scales administered by raters in clinical trials to ensure standardized assessments and data reliability. You will evaluate the quality of assessments, interact with raters to discuss methodologies, and provide necessary guidance. Additional responsibilities include assessing rater performance and assisting in communications related to the clinical trial.


Key Responsibilities:

  • Rater Interaction & Assessment Review:

    • Review and ensure the quality of clinical assessments to maintain data reliability.
    • Conduct live interactions with raters to discuss assessment methodology, scoring techniques, and provide necessary guidance.
  • Training & Calibration:

    • Participate in all required orientation, training, and calibration activities for clinical trials.
    • Be prepared to discuss relevant issues, scale items, and have necessary documents ready for rater interactions.
  • Documentation & Task Management:

    • Complete all rater interactions and assigned tasks as per the schedule.
    • Ensure timely submission of all necessary documentation.
  • Functional Assessments & Communication:

    • Perform functional assessments of rater performance, including mock interviews.
    • Assist in preparing and disseminating communications related to clinical trials.

Required Qualifications & Experience:

  • Education: Master’s degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing, Social Work, or a related field.

  • Experience:

    • Minimum of 3 years of experience administering psychiatric assessments, rating scales, or structured clinical interviews.
    • At least 3 years of clinical experience with psychiatric populations.
    • Minimum of 3 years administering scales in clinical research trials (excluding graduate/doctoral research work).
    • CNS (Central Nervous System) trials experience is preferred.
  • Skills:

    • Strong interpersonal skills with the ability to engage professionally with all levels of personnel and clientele.
    • Excellent organizational, time management, attention to detail, and problem-solving skills.
    • Proficiency in Microsoft Office and general computer systems.

Additional Requirements:

  • Fluency in English is required.
  • Native language proficiency is needed for the specific clinical trial language.

What We Offer:

  • Opportunities for professional growth in clinical research and assessment.
  • Competitive compensation and benefits.
  • The opportunity to contribute to impactful global health initiatives.

Equal Opportunity Employment: IQVIA is committed to diversity and inclusion, offering equal employment opportunities to all, including veterans and individuals with disabilities.

For more information, visit IQVIA Careers.


COVID-19 Vaccination Requirement: IQVIA requires employees to meet specific COVID-19 vaccination status requirements. For more details, visit COVID-19 Vaccine Status.