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Position: Senior Statistical Programmer
Institution: Cytel Inc.
Location: Germany
Duties: Providing significant technical expertise for statistical programming in all phases of programming support, developing automated reports and preparation of submission data standard packages; Supporting statistical programming activities for multiple and/or large/complex drug/vaccine clinical development projects; Development and execution of statistical analysis and reporting deliverables (e.g. safety and efficacy analysis datasets, tables, listings, figures); Design and maintenance of statistical datasets that support multiple stakeholder groups; Serving as key collaborator with statistics and other project stakeholders in ensuring that project plans are executed efficiently with timely and high-quality deliverables; Being able to serve as statistical programming point of contact and knowledge holder through the entire product lifecycle for the assigned protocol if/when called upon; Effective analysis and report programming development and validation utilizing global and TA standards and following departmental SOPs and good programming practices
Requirements: Bachelor’s degree or equivalent, preferably in a scientific discipline such as Statistics, Computer Science, Mathematics, etc; Minimum 10 years of SAS programming experience supporting clinical trials in the Pharmaceutical & Biotech industry; 5+ years of study lead experience working with cross functional teams, including leading programming teams; Minimum 3 years of recent experience supporting Oncology studies
   
Text: Senior Statistical Programmer Providing significant technical expertise for statistical programming in all phases of programming support, developing automated reports and preparation of submission data standard packages; Supporting statistical programming activities for multiple and/or large/complex drug/vaccine clinical development projects; Development and execution of statistical analysis and reporting deliverables (e.g. safety and efficacy analysis datasets, tables, listings, figures); Design and maintenance of statistical datasets that support multiple stakeholder groups; Serving as key collaborator with statistics and other project stakeholders in ensuring that project plans are executed efficiently with timely and high-quality deliverables; Being able to serve as statistical programming point of contact and knowledge holder through the entire product lifecycle for the assigned protocol if/when called upon; Effective analysis and report programming development and validation utilizing global and TA standards and following departmental SOPs and good programming practices Bachelor’s degree or equivalent, preferably in a scientific discipline such as Statistics, Computer Science, Mathematics, etc; Minimum 10 years of SAS programming experience supporting clinical trials in the Pharmaceutical & Biotech industry; 5+ years of study lead experience working with cross functional teams, including leading programming teams; Minimum 3 years of recent experience supporting Oncology studies
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