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Job Description
Seeking a Clinical SAS Programmer with expertise in statistical programming and methodology to collaborate with a global pharma company's Statistics team.
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 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
- 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