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
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
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
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
French Version Pour être éligible à ce poste, vous devez résider dans le même pays/la même région commerciale où se trouve lemploi Location: Canada, Télétravail Description de poste interne IQVIA recrute afin d’élargir son équipe FSP
