Senior Principal Statistical programmer (m/f/d)

Rahmendaten

<p><strong>Senior Principal Statistical Programmer (m/f/d)</strong><br> <br> Looking for an experienced Statistical Programmer to support Global Medical Affairs. The role focuses on conducting statistical analyses for publications, abstracts, presentations, conferences, as well as regulatory and pricing submissions. Work is based on a dynamic publication and submission plan provided by internal stakeholders.</p> <p> </p> <strong>Key Facts:</strong> <ul> <li><strong>Start:</strong> 22 Dec 2025 <li><strong>End:</strong> 31 Mar 2026 <li><strong>Workload:</strong> 40 hours/week <li><strong>Remote:</strong> 100% (within Europe) <li><strong>Travel:</strong> not required <li><strong>Extension:</strong> planned </ul> <p><br> <strong>Responsibilities:</strong></p> <ul> <li> <p>Conduct statistical analyses for Global Medical Affairs</p> <li> <p>Program SDTMs, ADaMs, and TFLs in <strong>SAS</strong> and <strong>R</strong></p> <li> <p>Perform QC/validation of SDTMs, ADaMs, and TFLs created by team members</p> <li> <p>Support publications, abstracts, presentations, conferences, and submission activities</p> <li> <p>Work according to a dynamic publication and submission plan<br>  </p> </ul> <p><strong>Requirements:</strong></p> <ul> <li> <p>Bachelor’s degree in statistics, biostatistics, mathematics, computer science or life sciences (Master’s in bio/statistics preferred)</p> <li> <p>Experience in clinical research, pharmaceutical, CRO, or medical device environment (incl. post-marketing / Phase IV)</p> <li> <p>Strong programming skills in <strong>SAS</strong> and <strong>R</strong></p> <li> <p>Experience with SDTMs, ADaMs, and CDISC standards</p> <li> <p>Experience in <strong>Phase IV Oncology</strong></p> <li> <p>Experience with <strong>Poolings</strong></p> </ul>