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

IQVIA; Paris; Sur place; EUR 90 000 - 120 000; Plein temps

Résumé du poste

IQVIA in Paris seeks a Principal Statistical Programmer to lead complex programming activities across studies, develop process methodologies, and provide internal consulting on specifications and user needs.

You will plan and coordinate integrated programming solutions, mentor SP team members, and ensure adherence to CDISC/ADaM/SDTM standards while collaborating with statisticians and clinical teams.

Qualifications

• Bachelor's degree or higher in a relevant field.
• 7+ years of statistical programming experience in life sciences.
• Strong efficacy experience.
• Advanced knowledge of statistics, programming and clinical drug development.
• Advanced knowledge of Base SAS, SAS Graph and SAS Macro.
• Advanced knowledge of CDISC/ADaM/SDTM.

Responsabilités

• Plan, coordinate, and implement programming for complex studies, including creation of tables, figures, and lists.
• Program analysis datasets and transfer files for clients.
• Perform programming QC checks and address data issues.
• Develop programming specifications from project requirements.
• Provide advanced technical expertise and lead project solutions for SP teams.
• Mentor SP team members and train colleagues.
• Communicate with statisticians and clinical teams to align requirements and timelines.
• Estimate scope, allocate resources, and negotiate timelines.

Connaissances

Statistical programming

Efficacy experience

Clinical drug development

SAS programming

CDISC/ADaM/SDTM knowledge

Formation

Bachelor's degree in Maths, CS, Statistics or related field

Outils

Base SAS

SAS Graph

SAS Macro

Description du poste

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.