EPM Scientific are currently partnered with a Pharmaceutical company running an exciting project. They are urgently seeking a Freelance Statistical Programmer to support their expanding biometrics team. See a short summary below: Contract Conditions: Start date: ASAP Location: Europe, Remote Contract Type: Freelance / Consultant - 1 FTE, 6-12 Months Contract Language: English Project: Submissions Key Responsibilities: Support integration of new trial data into existing analysis data pool. (Re-)Creation and validation of tables, figures, and listings (TFLs) for clinical trial reporting. Creation and QC of programming documentation (e.g., define.xml, reviewer's guide, and related deliverables). Ensure compliance with CDISC standards (SDTM, ADaM) and regulatory requirements. Collaborate closely with biostatisticians and data management teams to ensure accurate and timely deliverables. Troubleshoot and resolve programming issues, ensuring high-quality outputs for submission. Requirements: Bachelor's or Master's degree in Statistics, Computer Science, or related field preferred but not required. Strong experience in statistical programming within clinical trials (3 years preferred). Proficiency in SAS programming; experience with CDISC standards (SDTM, ADaM) is essential. Previous experience in Submissions highly desirable. If this role is of interest to you, please apply directly to learn more. If not, feel free to share with your network.