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    Lead Data Manager - Montréal, QC, Canada - ERGOMED

    ERGOMED
    ERGOMED Montréal, QC, Canada

    2 weeks ago

    Default job background
    Description
    Ergomed Group is a rapidly expanding full service mid-sized CRO specialising in Oncology and Rare Disease.
    Ergomed Group is a rapidly expanding full service mid-sized CRO specialising in Oncology and Rare Disease.
    Since its foundation in 1997 the company has grown organically and steadily by making strategic investments and landmark acquisitions, with operations in Europe, North America and Asia
    creative contribution and realistic career development.
    We have nourished a true international culture here at Ergomed.

    We value employee experience, well-being and mental health and we acknowledge that a healthy work life balance is a critical factor for employee satisfaction and in turn nurtures an environment from which a high-quality client service can be achieved.

    The Lead Data Manager (LDM) within the ERGOMED Data Management (DM) department is responsible for providing oversight of all DM parts of a project from study start-up to database lock by working in a collaborative team environment with all functional groups.

    The Lead Data Manager represents a position under direction of the Director of Data Management.
    Provide updates for Data Management during internal/client team meetings and communication if required.
    Provides metric reports for internal/external project team
    Meets with the Project Manager to work on completing the study objectives in a timely manner
    Provides training of other DM staff on project specific processes
    Provides feedback to other project team members and managers to improve the deliverables
    Authors or reviews data management documentation including the Data Management Plan,
    Data Review Plan, eCRF Completion Guidelines, and others as needed
    Supports design and testing of EDC study designs
    Communicates any project risks or possible quality issues to the Project Manager
    May work on projects across multiple trial EDC platforms
    Maintains project files and ensures full traceability of all processes and documentation
    Manages Lab ranges across the entire study
    Performs data management activities such as data review, serious adverse event reconciliation, third party electronic data (e.g. laboratory, PK, diary) reconciliation, and query management
    Oversees the issuing of queries and reviews query responses with the highest level of quality
    3-5 years of relevant experience in pharmaceutical industry and/or contract research organization, specifically in data management.

    Proficiency in computer applications:
    Windows, Excel, Word, Outlook etc.

    We prioritize diversity, equity, and inclusion by creating an equal opportunities workplace and a human-centric environment where people of all cultural backgrounds, genders and ages can contribute and grow.

    Training and career development opportunities internally
    Opportunity to work with colleagues based all over the world, with English as the company language
    Quality
    Seniority level Mid-Senior level

    Employment type Full-time

    Job function Information Technology

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