Freelance Statistical Programmer

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.