Statistical Programmer II (CVRM)

<p><span><span>Location: Warsaw, Poland</span><br /><span>Hybrid model of work: 3 days in office, 2 remote per week</span><br /><br /><span>Are you an experienced<b> Statistical Programmer II</b> with good knowledge of clinical drug development? Would you like to be part of a fast-paced and agile global team that has direct strategic impact on drug development, empowered and trusted to innovate and experiment? Join us at AstraZeneca CVRM (Cardiovascular Renal Metabolism) Biometrics to impact a wide range of engaging projects striving to make a difference for millions of patients. Our Biometrics team consists of Statisticians, Statistical Programmers, Information and Data Scientists. We drive and contribute to optimized clinical drug development programs and access to information and scientific knowledge management.</span></span></p><p><span> </span></p><p><span><span>We are now offering an exciting opportunity for a dedicated and highly motivated individual to join us in the role as a Statistical Programmer.</span></span></p><p><span> </span></p><p><span>The <b>Statistical Programmer II</b> is primarily responsible for providing support to deliver technical programming and <br />information components of moderate scope and medium complexity studies or drug projects. It will act as a contributor on <br />cross-functional teams to deliver continuous improvement. This role works under the general direction and support of an <br />experienced programmer.</span></p><p><span> </span></p><p><span><b>Accountabilities</b><br />• Under guidance, provides SDTM, ADaM, TFLs technical programming and information components of a project<br />• Understands the contents of protocols and clinical development plans to understand contribution of their work<br />• Works within established frameworks and ensures high quality is built into own deliverables<br />• Works independently for well-defined scope of work<br />• Continues to acquire knowledge of drug development process<br />• Continues to increase knowledge of SAS<br />• Continues to increase knowledge of industry standards<br />• Takes steps to understand the roles and skills of others in clinical study teams<br />• Takes steps to understand the roles and skills of other functions in drug development<br />• Proactively keeps the lead programmer updated on progress of deliveries</span></p><p><span> </span></p><p><span><span><b>Education, Qualifications, Skills, and Experience:</b></span></span></p><p><span>• Degree in Mathematical (i.e., Applied Math, Engineering, etc), Statistical, Computer Science, Life Science, or equivalent<br />• Intermediate programming skills<br />• Basic knowledge of the clinical development process</span></p><p><span> </span></p><p><span><span><b>Desirable Skills/Experience:</b></span></span></p><p><span>• Knowledge of industry standards<br />• Prior usage of a statistical/mathematical programming language</span></p><p><span> </span></p><p></p><p style="text-align:inherit"></p><p style="text-align:left"><b>Date Posted</b></p>27-mar-2026<p style="text-align:inherit"></p><p style="text-align:left"><b>Closing Date</b></p>29-kwi-2026<p></p><p></p><p>AstraZeneca embraces diversity and equality of opportunity.  We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills.  We believe that the more inclusive we are, the better our work will be.  We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics.  We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.</p>