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 in clinical trials. You will take part in statistical programming activities and manage clinical data submissions according to established CDISC specifications. This position may also include responsibilities for project timelines and mentoring the team in best practices.Key Responsibilities:Lead statistical programming for clinical trial submissionsDevelop and verify SAS programs for data analysis and conversionCreate specifications for statistical programming documentationTrain colleagues and support team developmentAdhere to SOPs for programming activitiesRequirements:Minimum 6 years in statistical programming rolesBachelor's in statistics, computer science, or life sciencesFamiliarity with CDISC (SDTM, ADaM) requirementsProficient in SAS programming and data analysisStrong organizational and project management skillsLeverage your statistical programming expertise to enhance clinical trial outcomes.

📌 Lead Statistical Programmer In Clinical Research (Quebec City)
🏢 Connect Life Sciences
📍 Quebec City