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 in either statistics
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
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
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,
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
Must be eligible to work in Canada without restrictions Must have lead experience Must have recent Oncology experience No 3rd parties Qualifications : Bachelors Degree, 6+ years of industry experience, along with extensive Oncology experience Job
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