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.

Responsibilities:

• 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