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    Job · 15512429

    Iqvia Biotech logo

    Medical Data Reviewer

    Iqvia Biotech · Bengaluru · onsite · Posted 49d ago

    Undisclosed2–7 yrsfulltimeSourced fromNaukri

    About a minute. You'll make an account on the way through.

    About this role

    Job Summary

    Review structured clinical patient data output without direct access to medical charts to ensure medical plausibility and to determine adherence to protocol and overall completeness and readiness of the supplied patient information for next level of review.

    Responsibilities

    • Identify any anomalies in patient reported data that require further investigation with the clinical site to determine overall accuracy
    • Review investigation product dosing records to determine adherence to protocol and identify possible inaccurate / missed dosages
    • Review all reported Adverse Events (AEs) to ensure all supporting information is expected and/or implausible data is verified. Review all reported Concomitant Medications to ensure no medication is disallowed per protocol, supports an existing reported medical condition or is prescribed for a reported AE
    • Review all inclusion and exclusion criteria to ensure each patient meets minimum level of acceptance into the clinical trial
    • Ensure proper end-of-study (EOS) information is correctly documented to determine primary reason for the patient ending participation in the clinical trial
    • Review all laboratory results to ensure completeness of information supplied, adherence to protocol schedule of events and determine if reported laboratory values represent a potential safety condition not reported in the AE information for the patient
    • Review all patient reported medical history information to verify completeness of reported information, adherence to protocol expectations and its impact on other patient reported/observed information (e.g., laboratory results, AEs, etc.)
    • Review additional information, as necessary, to determine overall readiness of the patient information for next level review
    • Review all supplied Line Listings to determine data accuracy across patients within a specified group of data points
    • Review status information and data flow reports and take appropriate actions
    • Serve as POC/ Back-up POC
    • Interact with other Medical review staff to verify/clarify information and/or triage new data issues or prior identified action items
    • Attend Kick-Off meetings, weekly team meetings, and client meetings, as needed or requested.

    Qualifications

    • BDS/MDS with 2 years of work experience
    • Understanding of clinical/medical data.
    • Background in Medical Terminology, Pharmacology, Anatomy, and Physiology
    • Excellent motivational, influencing and coaching skills
    • Ability to work on multiple projects and manage competing priorities
    • Strong customer focus skills
    • Ability to establish and maintain effective working relationships with coworkers, managers and clients


    Disclaimer: This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.

    Sourced from naukri

    Skills

    clinical researchFocuspharmacologyaesInvestigationHealthcaremanagementLife SciencesRecruitment

    About IQVIA Biotech

    Iqvia Biotech logo

    Iqvia Biotech

    Durham

    CA

    About

    IQVIA Biotech delivers specialized clinical development services, facilitating drug development for the pharmaceutical and biotech sectors.

    Industries

    BiotechnologyClinical TrialsHealth CareMedicalPharmaceutical

    Employee ratings

    23 reviews

    3.4/ 5

    Culture

    3.3

    Career growth

    2.8

    Work-life

    3.1

    Employees rate it well for

    Work Life Balance7Work Culture5Senior Management4

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    Medical Data Reviewer · waiting for your command