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Tier-1 brand, mid-level seniority, and metro/hybrid posting increase applicant competition.
Highly specialized clinical trial statistical programming limits transferability across industries.
Multiple mandatory filters: SAS, clinical trials expertise, ICH/regulatory knowledge and 3+ years experience.
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Deliver high-quality statistical programming outputs including analysis-ready datasets, tables, listings, and figures for clinical study reports and asset level deliverables.
Ensure adherence to programming standards and perform quality control and documentation throughout the study lifecycle for assigned deliverables.
Collaborate with statisticians and programming leads to clarify specifications and potentially contribute to development of study-specific or department-level programming standards.
Bachelor's or Master's degree in Statistics, Biological Sciences, IT, or related field.
Minimum of 3 years relevant experience in pharmaceutical, biotech, CRO, or Regulatory Agency environment.
Hands-on experience with Statistical Programming and SAS.
Knowledge of clinical trials data operations, ICH guidelines, regulatory standards, and relevant clinical data standards.
Experienced in delivering high-quality programming outputs independently with attention to detail and timelines in clinical trial settings.
Comfortable working in a hybrid work environment and collaborating closely with statisticians and programming leads.
Demonstrates ability to solve routine and occasionally complex programming problems with limited supervision and contributes to process improvement or standards development.