Principle Statistical Programmer

Experience: 10 - 15 Years

Location: Fully Remote

About the Company: A global pharmaceutical company

Your Main Responsibilities:

• Collaborates with other team members to provide programming support to deliver technical programming and information components of a study or a project deliverable

• Implements statistical programming aspects of the protocol or clinical development program

• Ensures high quality deliverables

• Programs independently with efficiency and quality

• Writes specifications

• Contributes to the development of best practices to improve quality, efficiency and effectiveness within function

• Delivery of the Clinical Study Report (CSR), Study Data Tabulation Model (SDTM)/Analysis Data Model (ADaM) databases and Tables, Figures and Listings (TFL) outputs, following applicable data standards and regulations

• Collaboration with study team members including but not limited to the statistician, lead programmer, data manager and study leader

Essential

• Degree in Mathematics (i.e., Applied Math, Engineering, etc), Statistics, Computer Science, Life Science or equivalent

• Extensive SAS programming knowledge and experience (SAS Base, Enterprise Guide, 4GL)

• Accomplished programming skills including macro language

• Intermediate knowledge of the clinical development process

• Good knowledge of industry standards

• Ability to apply programming knowledge to problem solving

• Ability to manage relevant documentation

Desirable

• Familiarity with CDISC, Study Data Tabulation Model (SDTM), Analysis Data Model (ADaM) standards

• Manage concurrent activities within their assigned study(ies) or project.