Sr. SAS Programmer
GW Pharmaceuticals
Toronto, CA
2d ago

We are looking for enthusiastic and talented individuals who thrive on challenge and change, and who want to make a difference through the delivery of results.

We are looking for enthusiastic and talented individuals who thrive on challenge and change, and who want to make a difference through the delivery of results.

We are continuing to build out our team and are looking for talented individuals dedicated to making a difference in the lives of our patients.

About the Role :

The Senior or Principal SAS programmer is responsible for SAS programming on clinical studies.

Acts as Lead SAS Programmer on individual studies, across related studies and for integrated summaries.

Responsibilities :

  • Review and monitor data received from data management to ensure suitability for reporting.
  • Assist in design of study databases (in SAS datasets) ensuring adherence to CDISC standards whilst creating databases that are amenable to processing within the Biometrics department either individually or as integrated summaries.
  • Programme of ad hoc queries on study databases to support data review.
  • Act as a SAS programming point of contact within GW.
  • Act as Lead SAS Programmer on clinical trials.
  • Review of deliverables from CROs, including review / validation of CDISC deliverables.
  • Perform quality control review of work completed by other members of the team.
  • Interact with report writers in the production of integrated clinical reports and other documents containing information from clinical study databases.
  • Interact with other disciplines to ensure successful execution of studies.
  • Input into the development of departmental processes, including standard working practices, operating procedures and implementation of CDISC.
  • Requirements :

  • Bachelors degree preferred, with strong CRO / Pharma experience.
  • Excellent working knowledge of SDTM and ADaM.
  • CDISC experience essential
  • Thorough knowledge of applicable regulatory requirements and guidelines, e.g. ICH Guidelines.
  • Proficient in the use of computers and especially the Windows operating system and Microsoft products.
  • Proficient in the use of the SAS system, especially SAS Base; experience of the use of SAS / Graph and SAS / Stat would be an advantage.
  • Familiar with data from clinical trials.
  • Able to work in a fast-paced, flexible, team-oriented environment.
  • Possess excellent interpersonal and communication skills (written and verbal).
  • Strong attention to detail with a view to bring studies to a quality conclusion.
  • Flexible, positive, creative thinker, good communicator.
  • Be able to work without close supervision. Well-developed time management skills are important.
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