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Senior Statistical Programmer New




Princeton, United States

United States





Not specified

Permanent | Full Time

Job Overview:Hiring for Senior Statistical Programmer (Remote) FSP: can be based anywhere in USA/ Canada #LI-REMOTE* Develop SAS programs for SDTM, ADaM, client-defined analysis datasets, Patient Profiles, Tables, Listings and Graphs in support of the Statistical Analysis Plan, posters, manuscripts, Integrated of Summary of Safety (ISS) and Integrated Summary of Efficacy (ISE)* Provide technical planning to include overseeing the set-up of key macros and SAS programs.* Act as a Lead Programmer for projects* Represent Statistical Programming at internal and client meetings* Act as a Statistical Programming consultant to clients and internal customers in related disciplines e.g. Clinical Data Management, Project Management and Medical Writing.* Demonstrate excellent problem solving skills, a proactive approach and a willingness to make decisions on a regular basis.* Ensure quality of personal work and the work of the team when acting as a Lead Programmer* Prioritize personal workload and that of teammates; perform work with minimal supervision* Work on complex problems where analysis of situations or data requires an evaluation of intangible variables; development of technical solutions to abstract problems which require the use of ingenuity and creativity.* Advise Senior Statistical Programming Staff of changes in scope of projects to enable the timely development of change orders.* Good experience with CDISC standards including Define.xml files.* Display a positive attitude at all times, promoting and contributing to good team spirit in a professional environment.* Review draft and final production runs for project to ensure quality and consistency.* Represent Statistical Programming during client audits ensuring study documentation is maintained and filed according to Covance by Labcorp processes.* Assist with interviewing and selection of potential candidates* Carry out all activities according to Covance by Labcorp SOPs working within the framework of the Quality management System and to Good Clinical Practice (GCP).* Provide ongoing training and mentoring within Statistical Programming to ensure thorough knowledge of the processes used and the ongoing technical development.* Perform other duties as requested by management.Education/Qualifications:Minimum Required:* BSc in a computing, life science, mathematical or statistical subject.* A high computing content is considered to be beneficial; however proven computing skills are most important.* Alternative academic qualifications or experience are assessed to ensure equivalent background.Experience:Minimum Required:* 5 - 8 years experience with proven SAS skills within a clinical trials environment.* Knowledge in all aspects of clinical trials from initial study set-up to study completion.* Full knowledge and understanding of the processes and procedures used within a Statistical Programming environment.* Able to identify training and development needs, opportunities for optimizing staff utilization and employing the most efficient practices.* Excellent organizational skills and the ability to delegate and prioritize work to meet tight deadlines while maintaining high standards* Self motivation and ability to work independently with minimum direction.* Excellent time management skills and the ability to work to tight deadlines whilst maintaining the highest standards of work.* Good interpersonal skills and the ability to communicate appropriately withal levels of staff and confidently with other disciplines and external clients.* A proactive approach to developing and maintaining effective working relationships with staff in other disciplines, often in other locations and in working to achieve consistent processes and standards across them.* A co-operative and team orientated approach.* Team leadership experience, as demonstrated by ability to organize and motivate project teams.

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