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Tier-1 biotech brand and metro location increase competition despite niche biostatistics skillset.
Strong clinical trial and regulatory focus makes skills highly domain-specific to pharma/biotech.
Requires 8+ years, advanced SAS, regulatory submission experience and leadership — tight mandatory filters.
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Lead and manage an offshore team of Study Lead Programmers and Study Programmers to deliver end-to-end statistical programming activities for one or multiple products.
Accountable for successful execution and delivery of global programming milestones, analysis deliverables, and regulatory submission packages for assigned product areas.
Collaborate with Global Programming Lead to implement programming strategies and manage resource plans and budgets at the product level.
Bachelor’s degree or higher in biostatistics, statistics, mathematics, computer science, or related quantitative/scientific field.
At least 8 years of statistical programming experience in a clinical development environment.
Advanced skills in SAS programming including SAS/STAT, Macro, Graph, SQL, etc.
Strong leadership and communication skills with experience managing global offshore teams and prior regulatory submission experience.
Experienced leader capable of managing and growing offshore statistical programming teams with demonstrated project management skills.
Proven track record of handling complex programming tasks for clinical trials including regulatory submissions and ensuring data quality compliance.
Comfortable working across different time zones and collaborating in globally dispersed, cross-cultural teams, with a strategic focus on digital transformation and automation technologies.