Required skills: Minimum 6 years’ experience as a statistical programming working on clinical trials. Good knowledge of TFL programming. Experience in programming according to CDISC standards (SDTM, ADaM), and preparing documents for submission (Reviewer’s Guide, Define.xml) Attention
Senior/Principal Statistical Programmer | Small CRO | Remote Were partnered with a small CRO who are experiencing a large amount of growth within Biometrics. The Role: As a Senior Statistical Programmer, youll lead high-impact projects, tackling complex statistical programming tasks and
Elevate your career as a Senior Statistical Programmer in clinical trials with extensive SAS experience. Contribute to TFL programming and enhance submission processes using CDISC standards. In this role, you will leverage over six years of statistical programming experience
We are seeking a well-rounded Statistical Programmer to join a fast-moving clinical programming team supporting multiple clients and study types. This is a client-facing role requiring strong communication skills alongside deep technical expertise. The ideal candidate is adaptable,
Key Responsibilities Develop and validate complex analysis datasets (ADaM) and TFLs using SAS. Write and review programming specifications and supporting documentation. Create standard macros and tools to improve efficiency. Serve as a project lead programmer , assigning
Key Responsibilities Develop and validate complex analysis datasets (ADaM) and TFLs using SAS. Write and review programming specifications and supporting documentation. Create standard macros and tools to improve efficiency. Serve as a project lead programmer , assigning
