Interim Statistical Programmer
JCR Europe B.V.
| Company | JCR Europe B.V. |
| Category | Engineering |
| Location | NL |
| Remote | — |
| Employment | Not stated |
| Level | Not stated |
| Salary | Not stated by the employer |
| First seen | 2 Aug 2026 (the employer did not state a posting date) |
| Last verified | 9 Aug 2026 |
| Source | The employer's own careers page (company_site) |
Description
You support statistical programming activities across clinical trials and real-world evidence studies, with a strong emphasis on CDISC standards and regulatory submissions (MAA, BLA). You will lead and coordinate statiscal programming activities for regulatory submission (e.g. MAA, BLA). You will perform QA and validation of statistical programmin deliverables. You will be part of the Biostatistics team. You do have experience with regulatory submissions and associated components, preferably both on the CRO and sponsor site. You have a deep understanding of regulatory submission requirements, including ISS/ISR, SCS/SCE, and eCTD structureYou do have strong knowledge of CDISC standards (CSDTM, ADaM).You are fluent in English. Working in a great team of professionals with a drive to bring a product to patients. Please indicate your availability (as of when and how many hours a week) and your hourly/daily rate