Job Description
Clinical SAS ProgrammerOur 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 plansAccountable 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 createdCollaborate with data sciences in the planning and implementation of data quality assurance plansEffectively justify methods selected and implement previously outlined analysis plansConduct peer-review of work products from statistical colleaguesMaintain proficiency with respect to statistical programming and statistical methodology and in applying new and varied methodsMaintain current knowledge of CDISC data standardsEffectively utilize current technologies and available tools for conducting the clinical trial analysisCommunication of Results and InferencesCollaborate with other statistical colleagues to write reports and communicate resultsBe responsible for assisting in the communication of study results via regulatory submissions, and manuscripts, as well as for communicating one-on-one with key customersAssist or respond to regulatory queries working in collaboration with other statistical colleaguesUnderstand relevant disease states and competitive landscapes in order to enhance the level of customer focus and collaborationEnsure replication of tools and systems, where applicable, and stay informed of technology advancesPerform work in full compliance with assigned curriculum(s) and be responsible for following applicable corporate, medical, local, and departmental policies, procedures, processes and trainingRequirements:M.S., Ph.D., or equivalent experienceStatistics, Biostatistics, Computer Science5+ years of relevant experience that includes 3 years in major pharmaExperience in all major phases of drug development which includes immunologyProficiency in a statistical programming language(s)Regulatory response experience that is an assetHigh level of expertise in programmingInterpersonal/teamwork skills for effective interactionsTechnical growth and application with working knowledge of statistics and statistical softwareSelf-management skills with a focus on results for timely and accurate completion of competing deliverablesCreativity and innovationDemonstrated problem solving ability and attention to detailData analysis, technology, and systems expertise #J-18808-Ljbffr