Senior Statistical Programmer

0 years

0 Lacs

Posted:4 days ago| Platform: Linkedin logo

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Work Mode

On-site

Job Type

Full Time

Job Description

Summary

  • Responsible for all statistical programming/data review reporting and analytics development aspects of assigned studies or project-level activities. Acts as a key contributor in ensuring that drug-development plans are executed efficiently with timely and high quality deliverables.

About The Role

Major accountabilities:

  • Responsible for planning, monitoring, documenting of projects and analysis of information -Co-ordinate activities of all programmers either internally or externally assigned to the study/project work -Contribute to project level standards -Review and discuss data structures and participate in data review activities.
  • Responsible for development of programming specifications of analysis datasets or user requirement documentation -Contributes to some cost center goals and objectives -Broadens technical knowledge via departmental activities, literature reading and experiential learning.
  • May train junior.
  • new team members -Skilled in collaboration across project team(s) -Responsible for quality control and audit readiness of all assigned statistical programming deliverables as well as accuracy and reliability of statistical analysis results -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.
  • Innovative & Analytical Technologies.
  • Regulatory Submissions.
  • Data Management & Systems.
  • Statistical Programming.
  • Clinical Trial Design, Data Review & Reporting.

Skills

  • Clinical Trials.
  • Computer Programming.
  • Data Analysis.
  • 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

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