LGT Capital Partners

Senior Statistical Programmer

14 June 2024
Apply Now
Deadline date:
£57000 - £106000 / year

Job Description

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.


Job Description

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 -Make statistical programming/data review reporting development recommendations at study level.
  • Contribute to project level standards -Review and discuss data structures and participate in data review activities.
  • Provide input into statistical programming/data Reporting & Analytics solutions and/or ensure their efficient implementation -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:

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


  • NA.

Languages :

  • English.


Skills Desired

Clinical Trials, Computer Programming, Data Analysis, Management Reporting, Programming Languages, Statistical Analysis