As a Senior Statistical Programmer I, you will lead statistical programming deliverables for regulatory submissions, including specification and delivery of datasets, outputs, and responses to regulatory questions. You will also contribute to the statistical programming thinking, analysis, and reporting to relevant groups in product and study teams. Additionally, you will measure compliance to standards and automation use, employ good project management practices when planning and leading delivery, and hold CRO/Partners accountable for the high-quality standards of their deliverables.
Essential Skills/Experience:
Degree in Mathematics (i.e., Applied Math, Engineering, etc.), Computer Science, Statistics, Life Sciences or similar area
Strong experience in clinical drug development or healthcare
Advanced SAS Programming, CDISC standards knowledge and industry best practices
Excellent interpersonal skills
Desirable Skills/Experience:
Experience working in the Respiratory or Immunology therapeutic area
Other programming languages e.g., S-PLUS, R, Python, XML etc.
Extensive knowledge of Pinnacle 21 Validator
When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines.
In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That’s why we work, on average, a minimum of three days per week from the office
But that doesn't mean we’re not flexible. We balance the expectation of being in the office while respecting individual flexibility
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