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Statistical Programmer, Real World Evidence

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Primary Location: Durham, North Carolina, United States Additonal Locations: Cambridge, MA,USA; Kirkland, Canada,CAN; Mississauga, ON,CAN; New York, NY,USA; Toronto, ON,CAN Full time R1278735

Job description

Join us on our exciting journey!

IQVIA™ Real World Evidence (RWE) teams work with clients to help them collect and use real-world data to generate evidence to meet the needs of regulators, payers, providers, and patients.

Our approach is unique in the industry and is defining the way companies develop and apply real-world evidence for healthcare decision making.

We are collaborative, intellectually curious, entrepreneurial, and constantly looking for opportunities to harness the value of real-world evidence in an evolving industry.

Overview:

We, IQVIA, have one of the largest Biostatistics and RWE departments within the industry, and due to continued growth, we are seeking new brave minds to join our team.

You will utilize the SAS programming language to develop and maintain programs for clinical study report materials according to the objectives of a clinical trial for regulatory submissions. Programming and performing related tasks serving the full spectrum of statistical programming needs.

Statistical Programming Overview:

  • Import data from various sources

  • Program quality control checks for source data and reporting data issues

  • Interpret project level requirements and develop programming specifications

  • Write programming code following established Good Programming Practices

  • Program SDTM and ADaM datasets

  • Program to create statistical analysis tables, listing and figures

  • Validate datasets and all statistical outputs per prescribed gate checks

  • Communicate with internal and client statisticians and clinical team members to ensure appropriate understanding of requirements and timelines

  • Use and promote the use of established standards, SOPs, and standard methodologies

  • Provide training and mentoring to team members and department staff

You can help us bring clinical trial statistical analysis into the next generation. 

Award winning and innovative; we will give you access to cutting-edge in-house technology, allowing you to work on global projects across a variety of therapeutic areas. 

Be challenged in a fast-paced team environment that is collaborative in performing biostatistical analyses and statistical programming. 

Development opportunities and mentoring at all levels enable you to progress your long-term career in the direction you choose.

Requirements:

  • BSc or MSc in Biostatistics, Statistics, Mathematics, or Computer Science, with relevant experience

  • Experience in programming in SAS within the CRO/Pharma/Biotech/Healthcare industries

  • Knowledge of statistics and exhibit routine and occasionally complex analytical skills

  • A good understanding of Good Clinical Practice and ICH guidelines

Embrace your curiosity and grow your career in an exciting environment where development is a priority.

Think boldly and disrupt conventional thinking.

Enjoy what you do.

Discover a career with greater purpose and help create a healthier world.

Whatever your career goals, we are here to ensure you get there!

At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com

We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities.

https://jobs.iqvia.com/eoe

As the COVID-19 virus continues to evolve, IQVIA’s ability to operate and provide certain services to customers and partners necessitates IQVIA and its employees meet specific requirements regarding vaccination status.

https://jobs.iqvia.com/covid-19-vaccine-status

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