For one of our clients in the pharmaceutical industry, we're looking for a freelance Biostatistician.
Step into a biotech environment where data drives every decision and patient impact is real. As the lead statistician on high‑visibility trials, you’ll shape study strategy, translate numbers into insights for regulators, and keep external CRO teams humming, all while seeing your work accelerate life‑changing therapies.
What will be your assignment?
Craft optimal study designs and endpoints, then author and execute robust SAPs
Generate, validate and interpret TLFs for Phase I–IV trials
Direct CRO statisticians/programmers and partner daily with data management, clinical ops and medical writing
Own statistical deliverables for regulatory submissions and field agency questions
Who are you?
A Master's degree or PhD in (Bio)Statistics
3 or more years of experience within clinical trails
Strong know-how of complex Phase I‑IV methods and current regs (ICH, CDISC, 21 CFR Part 11)
Advanced SAS skills and fluency in CDISC SDTM/ADaM
Fluent in English
Ability to keep projects moving
Our offer
Project duration: end of 2025 (extension possible!)
Possibility to work fully remote
International environment