Principal Statistical Programmer - FSP (Permanent Homebased) m/w/d

IQVIA

Barcelona

Presencial

EUR 70.000 - 110.000

Jornada completa

14 días+

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Descripción de la vacante

IQVIA is seeking a Principal Statistical Programmer to provide advanced technical expertise across complex studies, planning integrated programming solutions, and delivering statistical tables, figures and lists.

You will act as technical team lead, coordinate requirements with statisticians and clinical teams, mentor SP staff, and ensure adherence to CDISC/ADaM/SDTM standards while managing scope and timelines.

Formación

  • Bachelor's degree in maths, computer science, statistics or related field.
  • 7+ years’ statistical programming experience in life sciences.
  • Strong efficacy experience.
  • Advanced knowledge of statistics, programming and drug development processes.
  • Advanced knowledge of Base SAS, SAS Graph and SAS Macro; CDISC/ADaM/SDTM.

Responsabilidades

  • Plan, coordinate, and implement programming for complex studies (tables, figures, lists).
  • Program analysis datasets and transfer files for internal/external clients.
  • Perform programming QC checks and report data issues.
  • Develop programming specifications from project requirements.
  • Provide advanced technical expertise and deliver project solutions.
  • Lead technical aspects for single/multiple complex studies and mentor SP staff.
  • Communicate with internal and client statisticians to align timelines and requirements.
  • Estimate scope, manage resources, and negotiate timelines for deliverables.
  • Promote standards, SOPs, and best practices in programming.
  • Provide training and mentoring to SP team members.

Conocimientos

Statistical programming
SAS programming
Project leadership
Stakeholder communication
CDISC/ADaM/SDTM
Clinical drug development
Data analysis datasets

Educación

Bachelor's degree in Maths/CS/Statistics

Herramientas

Base SAS
SAS Graph
SAS Macro

Descripción del empleo

Job Overview

As a Principal Statistical Programmer you will provide advanced technical expertise to develop process methodology for the department to meet internal and external clients’ needs, across complex projects and studies. This involves planning and coordinating the development of integrated programming solutions, serving the full spectrum of statistical programming needs. You will provide internal consulting services, including specifications and user needs analysis for complex project or client requirements.

Key Responsibilities
  • Perform, plan, coordinate, and implement the following for complex studies: programming, testing, and documentation of statistical programs for creating statistical tables, figures, and lists.
  • Program analysis datasets (derived datasets) and transfer files for internal and external clients.
  • Perform programming quality control checks for the source data and report data issues periodically.
  • Interpret project-level requirements and develop programming specifications for complex studies.
  • Provide advanced technical expertise and independently bring project solutions to SP teams.
  • Fulfill project responsibilities at the level of technical team lead for single complex studies or a group of studies.
  • Communicate directly with internal and client statisticians and clinical team members to ensure appropriate understanding of requirements and project timelines.
  • Estimate programming scope of work, manage resource assignments, communicate project status, and negotiate/re-negotiate project timelines for deliverables.
  • Use and promote established standards, SOP, and best practices.
  • Provide training and mentoring to SP team members.
Requirements
  • Bachelor's Degree in Maths, Computer Science, Statistics, or related field.
  • 7+ years’ Statistical Programming experience within the Life Science Industry.
  • Strong Efficacy experience.
  • Advanced knowledge of statistics, programming and/or clinical drug development process.
  • Advanced knowledge of computing applications such as Base SAS, SAS Graph, and SAS Macro.
  • Advanced knowledge of relevant Data Standards such as CDISC/ADaM/SDTM.
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