Job Description
Clinical SAS Programmer Our client, a global pharma company, is growing their Statistics team and is 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 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 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 Requirements: M.
S., Ph.
D., or equivalent experience Statistics, Biostatistics, Computer Science5+ 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 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
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