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    Principal Statistical Programmer

    REQ-10031239
    12月 04, 2024
    India

    摘要

    -Responsible for all statistical programming/data review reporting and analytics development aspects of several studies, a medium to large sized project or project-level activities. Acts as a key collaborator and strategic partner in ensuring that drug-development plans are executed efficiently with timely and high quality deliverables. Complies with project / study standards and specifications following internal and regulatory guidelines. Oversees programming style, quality of statistical reporting & compliance with timelines.

    About the Role

    Major accountabilities:

    • Lead statistical programming activities for several studies or drive the implementation of data analytics reports -Make decisions and propose strategies at study or project level.
    • May act as functional manager for local associates including providing supervision and advice on functional expertise and processes.
    • Build and maintain effective working relationship with cross-functional teams, able to summarize and discuss status of deliverables and critical aspects (timelines, scope, resource plan), e.g. as representative in study or project-level team.
    • Ensure project-level standardization -Provide and implement programming solutions; ensure knowledge sharing.
    • Act as expert in problem-solving aspects.
    • Ensure timely and quality development and validation of datasets and outputs for regulatory submissions/interactions, safety reports, publications, post-marketing activities etc -Leads/co‐leads novel projects within the team -Generates innovative ideas within own team and /or project team /functional community -Recognizes and leverages innovation opportunities for own team across projects -Mentors and inspires others to solve problems -Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt -Distribution of marketing samples (where applicable)

    Key performance indicators:

    • Achieve high level of quality, timeliness, cost efficiency and customer satisfaction across functional activities and deliverables.
    • Adherence to Novartis policy and guidelines -Customer / partner feedback and satisfaction

    Minimum Requirements:
    Work Experience:

    • Biostatistics.
    • Clinical Research Phases.
    • R&D Portfolio Management.
    • Statistical Programming.
    • Data Management & Systems.
    • Regulatory Submissions.
    • Innovative & Analytical Technologies.
    • Clinical Trial Design, Data Review & Reporting.

    Skills:

    • Classification Systems.
    • Clinical Trials.
    • Computer Data Storage.
    • Computer Programming.
    • Cross-Functional Teams.
    • Data Analysis.
    • Data Structures.
    • Initiative.
    • Programming Languages.
    • Reporting.
    • Statistical Analysis.

    Languages :

    • English.

    Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? http://www.novartis.com/about/strategy/people-and-culture

    Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: http://talentnetwork.novartis.com/network

    Benefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: http://www.novartis.com/careers/benefits-rewards

    A female Novartis scientist wearing a white lab coat and glasses, smiles in front of laboratory equipment.
    REQ-10031239

    Principal Statistical Programmer

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