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Clinical SAS Programmer

Reference:SCA013587 Location: Cork
Qualification:DegreeExperience:4-5 Years
Job Type:PermanentSalary: Not Disclosed
May be suitable for: SAS programmer

Clinical SAS Programmer
Our client, a global pharma company, are growing their Statistics team and are currently recruiting for a Clinical SAS Programmer to join their team on a permanent basis. This role will have hybrid working.


  • Collaborate with other statistical colleagues and study personnel to provide input to statistical analysis plans
  • Accountable for selecting statistical methods for data analysis, authoring the corresponding sections of the data analysis plan, creating the reporting database, and conducting the actual analysis once a reporting database is created
  • Collaborate with data sciences in the planning and implementation of data quality assurance plans
  • Effectively justify methods selected and implement previously outlined analysis plans
  • Conduct peer-review of work products from statistical colleagues
  • Maintain proficiency with respect to statistical programming and statistical methodology and in applying new and varied methods
  • Maintain current knowledge of CDISC data standards
  • Effectively utilize current technologies and available tools for conducting the clinical trial analysis
  • Communication of Results and Inferences
  • Collaborate with other statistical colleagues to write reports and communicate results
  • Be responsible for assisting in the communication of study results via regulatory submissions, and manuscripts, as well as for communicating one-on-one with key customers
  • Assist or respond to regulatory queries working in collaboration with other statistical colleagues
  • Therapeutic Area and Systems Knowledge
  • Understand relevant disease states and competitive landscapes in order to enhance the level of customer focus and collaboration
  • Ensure replication of tools and systems, where applicable, and stay informed of technology advances
  • Regulatory Compliance
  • Perform work in full compliance with assigned curriculum(s) and be responsible for following applicable corporate, medical, local, and departmental policies, procedures, processes and training

  • M.S., Ph.D., or equivalent experience
  • Statistics, Biostatistics, Computer Science
  • 5+ years of relevant experience that includes 3 years in major pharma
  • Experience in all major phases of drug development which includes immunology
  • Proficiency in a statistical programming language(s)
  • Regulatory response experience that is an asset
  • High level of expertise in programming
  • Proficiency in a statistical programming language(s)
  • Interpersonal/teamwork skills for effective interactions
  • Technical growth and application with working knowledge of statistics and statistical software
  • Self-management skills with a focus on results for timely and accurate completion of competing deliverables
  • Creativity and innovation
  • Demonstrated problem solving ability and attention to detail
  • Data analysis, technology, and systems expertise
For miore information please contact Sinéad Cullen on +353879500821 or [email protected]