Senior Statistical Programmer I/II

Location: Warsaw, Poland
Play a critical role in making our pipeline accessible to patients.

AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialization of prescription medicines for some of the world’s most serious disease. But we’re more than one of the world’s leading pharmaceutical companies.

We work on some of the most complex and interesting challenges. A fast-paced and agile team, we are empowered and trusted to innovate and experiment. With access to our extensive capabilities and comprehensive pipeline, you’ll be involved in countless submissions and a wide range of engaging projects along the complete drug development process.

The Role

You will provide Statistical Programming support and/or lead all programming related activities of the analysis and reporting process including, but not limited to, CSR development, regulatory submissions, commercialization and the scientific utilization of our data for AstraZeneca products.  There are many career options you can pursue for progression including technical pathways, management of global projects or line management.

You will work in the Programming department that not only oversees and delivers the programming aspects of analysis and reporting but also manages and maintains our end to end standards and our analysis and reporting production tools.

Main Duties and Responsibilities

Reporting to the Director within the Statistical Programming group you will provide programming expertise in one or more of the following areas:

• Creates/validates SDTM & ADaM datasets including dataset specification component 

• Creates/validates safety & efficacy TFLs

• Ensures high quality is built into own deliverables but also deliverables of other programmers 

• Programs independently with efficiency and quality

• Fluency in implementing good programming practice

• Initiaties/plans or leads team activities and tasks is additional asset

• Experience in leading the programming deliverables of a clinical study or a small to medium size project is additional asset

Requirements:

To succeed in this role, you’ll be an experienced programmer with good knowledge of technical and regulatory requirements related to programming within the pharmaceutical or healthcare industry.

• Degree  in Mathematical (i.e., Applied Math, Engineering, etc), Statistical, Computer Science, Life Science, or equivalent

• Very good SAS programming skills (at least 5 years of experience)

• Good knowledge of industry standards (SDTMs, ADaMs)

• Good project management skills

So, what’s next?

• Are you ready to bring new ideas and fresh thinking to the table? Brilliant! We have one seat available and we hope it’s yours.