Senior Clinical Data Standards Director

1 day ago


Vancouver, British Columbia, Canada Xenon Pharmaceuticals Inc. Full time
Unlock Career Advancement Opportunities at Xenon Pharmaceuticals Inc.

We are seeking an exceptional Senior Clinical Data Standards Director to join our dynamic team at Xenon Pharmaceuticals Inc. This role offers a unique opportunity to leverage your expertise in clinical data standards, programming, and technical leadership to drive excellence in our clinical trials.

About the Role:

The Senior Clinical Data Standards Director will be responsible for providing expert-level principal programming support and technical leadership to develop, maintain, validate, and run SAS computer programs that access, visualize, and report clinical trial data. As a key member of our team, you will work closely with cross-functional teams to define and implement data visualization environments, improve process efficiencies, and create data visualizations to present clinical data effectively.

Key Responsibilities:

  • Lead and manage all Clinical Programming activities on project or study level using eDC and external raw data
  • Work cross-functionally to define and implement a data visualization environment, enabling data review for medical monitoring and clinical analysis
  • Lead efforts to programmatically improve the efficiencies of CDMs 'processes as they relate to data monitoring and cleaning
  • Create data listings to support ongoing Medical Monitoring review of data, specifically AE data to facilitate AEs/Events of Special Interest adjudication
  • Contribute to the development and review of Standard Operating procedures (SOPs), related to clinical data management programming

Requirements:

  • A minimum of 5 years' experience in a data management programming lead position
  • Knowledge of multiple phases of clinical development and experience in using SAS, or equivalent programming language, for clinical trials
  • Hands-on experience and in-depth knowledge in CDISC standards is preferred
  • Excellent knowledge of SAS/Macro, SAS/SQL, SAS/GRAPH, and SAS/STAT
  • Experience in CNS, pediatric rare disease area preferred

Compensation and Benefits:

We offer a competitive compensation package including a base salary range of $153,200 to $209,000 CAD, target bonus, stock options, and a full range of benefits including medical, dental, vision, short-& long-term disability, accidental death & dismemberment, and life insurance programs, Employee Assistance Program, travel insurance, and retirement savings programs with company matching contributions.



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