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    Job · 16241927

    Iqvia Biotech logo

    Sr Clinical DB Designer

    Iqvia Biotech · Hyderabad · onsite · Posted 45d ago

    Undisclosed7–12 yrsfulltimeSourced fromNaukri

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

    About this role

    Job Summary

    Responsible for study build design, edit specifications, system configurations and is accountable for associated study design components. This role will collaborate with various stakeholders- DTL, Programmer, Validation Team, vendors, statisticians, and client representatives. In addition to project deliveries, the role also would be responsible for the project financials from programming shared services perspective.

    Responsibilities

    • Interprets the study protocol.
    • Design and update the eCRF using third party or in house CDMS tools in alignment with industry standards like SDTM, CDASH as applicable.
    • Create and update Edit Specification Document.
    • Generate specifications for EDC build components (e.g., Rights and Roles, System Settings and Home Page)
    • Complete the Study Authorization Form and Trial Capacity Request Form (InForm)
    • Attend the Pre-Design Meeting, Online Screen Review Meeting, Unblinded Data review meeting. Attend and present comments at the Internal Design Review Meeting. May lead Online Screen Review Meeting.
    • Facilitate the internal Edit Specification Review Meeting and leads the discussions regarding the Edit Specification Document.
    • Design the database to collect LLRR data within the InForm database and ensure Rights and Roles document has appropriate access for Entry and Updates.
    • Communicate any project risks to the Data Team Lead, including the potential for missing a timeline in the Data Management Project Plan.
    • Escalate potential quality issues.
    • Ensure the completion and documentation of all project-specific training, as well as staying current with required Standard Operating Procedures.
    • Reviews build timelines and provide input as applicable.
    • Reviews QIP for own projects, identify out of scope activities if any and inform relevant parties.
    • Responsible for multiple study design projects at the same time.
    • Might be working on projects across multiple platforms.
    • Identify areas for process improvements on an ongoing basis. Actively take part and contribute towards process improvement initiatives as assigned besides providing suggestions for continuous improvement of processes.
    • All responsibilities are essential job functions unless noted as nonessential (N).

    Qualifications

    • Bachelors Degree Bachelor in Science/Computer science/Information Technology or Bachelor in Technology Req
    • 7+ years of relevant core Technical designer experience


    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

    Shared Servicesclinical researchProgrammingSdtmProgrammerProcess ImprovementQIPData ReviewHealthcareResearchData ManagementInformation TechnologyLife Sciences

    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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    Sr Clinical DB Designer · waiting for your command