Senior Statistical Programmer

No 3rd party candidates

• Recent small to midsized pharma/biotech experience required – no recent CRO experience)
• Long term experience at most roles (2+ years)
• Recent Oncology experience

Responsibilities:

• Provide Statistical Programming support either in the form of production or verification of SAS scripts and outputs for Analysis Files, Tables, listings, Figures, and any other form of Clinical Trial in addition to writing analysis file specifications and other relevant documentation of deliverables and analysis methods.
• Ensure effective planning to meet quality and timely delivery of deliverables.
• Comply with project/study programming standards and specifications following internal guidelines.
• Ensure accuracy of clinical trial results for internal and external audiences (e.g., regulatory authorities, academic community, and healthcare providers) via biometrics QC of documents with clinical data.
• Programming support for relevant deliverables, such as Investigator Brochures, publications, US and ex-US regulatory submissions.
• Hands-on programming of in-house deliverables.
• Verification Review of Statistical Analysis Plans, documents, spreadsheets, slides for in-house presentations and external publications.

Required:

• MS, BS/BA degree or other suitable qualification with relevance to the field.
• Oncology experience.
• 10+ years of statistical programming experience with clinical trial data using SAS software.