Sr Manager, Statistical Programmer

Responsibilities :

• Provides leadership / expertise in day-to-day statistical programming in support of ongoing projects.
• Develops and / or validates SAS programs to generate SDTM / ADaM datasets following industry standards, regulatory requirements, and statistical instructions.
• Develops and / or validates SAS programs to generate statistical output (e.g. TLFs) of clinical trial data as specified in the Statistical Analysis Plan (SAP), as required for regulatory and safety review reasons (i.e. DSUR or IDMC deliverables), and for ad hoc analysis as requested.
• Documents data and programming information in accordance with SOPs, guidelines and industry standards.
• Manages timelines for statistical programming activities.
• ssists the Head of Statistical Programming in developing templates for derived dataset specifications, programming specifications, and other supporting documents.
• Develops SAS macros, templates and utilities for reporting and data cleaning.
• Oversees and manages Contract Research Organizations (CROs).
• Develops and tests SAS codes for clinical trial database logic checks.
• ssign tasks to and monitor timelines for junior programmers.

Requirements :