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      Senior Principal Statistical Programmer

      REQ-10044706
      3月 17, 2025
      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? https://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: https://talentnetwork.novartis.com/network

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

      A female Novartis scientist wearing a white lab coat and glasses, smiles in front of laboratory equipment.
      REQ-10044706

      Senior Principal Statistical Programmer

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