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

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:
The programming testing and documentation of statistical programs for use in creating statistical tables figures and listing
The programming of analysis datasets (derived datasets) and transfer files for internal and external clients
The programming quality control checks for the source data and to report the data issues periodically
Ability to interpret project level requirements and develop programming specifications as appropriate for complex studies.
Provide advanced technical expertise in conjunction with internal and external clients and independently bring project solutions to SP teams
Fulfil project responsibilities at the level of technical team lead for single complex studies or group of studies.
Directly communicate 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/renegotiate project timelines for deliverables
Use and promote the use of established standards SOP and best practices
Provide training and mentoring to SP team members

Requirements:

Bachelors 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
Language
Advanced knowledge of relevant Data Standards (such as CDISC/ADaM/SDTM)

Join IQVIA to see where your skills can take you

Global exposure
Variety of therapeutic areas
Collaborative and supportive team environment
Access to cuttingedge and innovative inhouse technology
Excellent career development and progression opportunities
WorkLife Balance with a strong focus on a positive wellbeing

Unleash your potential!
It takes passion to make the extraordinary possible for patients. Our culture of innovation and collaboration enables us to explore new possibilities and help improve health around the world.
When you join our diverse global team youll harness the power of unparalleled data advanced analytics cuttingedge technologies and deep healthcare and scientific expertise to drive healthcare forward

IQVIA is a leading global provider of clinical research services commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at