Clinical Statistical Programmer - Biotech & Contract Research Organization (CRO) An internationally recognized Contract Research Organization (CRO) that collaborates with leading pharmaceutical and biotechnology companies to accelerate the development of innovative treatments. For over 35 years, this company
Step into a Lead Statistical Programmer position focused on clinical research and impactful data submission. Use your extensive TFL programming knowledge to ensure compliance with CDISC standards. This role seeks a dedicated programmer with over six years of experience
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) A bachelor’s degree
Senior/Principal Statistical Programmer | Small CRO | Remote/Hybrid 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
We are seeking an experienced Senior Statistical Programmer with strong oncology and Health Technology Assessment (HTA) experience to support clinical development and evidence-generation activities. The ideal candidate will have a strong background in statistical programming, clinical trial data standards,
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