Senior Statistical Programmer

The Aixial Group is an International Contract Research Organization (CRO), a member of the ALTEN Group, providing complex services in clinical trials (phase I-IV) and non-interventional studies. Our offices are located in France, UK, US, Belgium, Czech Republic, Switzerland, Denmark, Romania, and India. The CRO occupies a unique position in the clinical research industry, not only as an expert in the operational delivery of clinical trials in complex disease areas including oncology, immuno-oncology, and cell therapy, but also as a developer of its own technologies for managing clinical data. This is a very exciting time to join as we are at the cutting edge, defining new and more efficient ways to design, capture, manage, review, and visualize clinical trial data. We are currently looking for an enthusiastic and talented Senior Statistical Programmer willing to be involved in all spectrum of Statistical Programming activities, including acting as Lead Programmer on studies. This role can be home-based in the UK or EU where we have the ability to hire. Your core responsibilities:Creation and QC of study specifications for SDTM datasets, and statistical programming and QC of SDTM datasets for Phase I-IV trials.Creation and QC of study specifications for ADaM datasets, and statistical programming and QC of ADaM datasets for Phase I-IV trials.Statistical programming and QC of tables, listings and figures for Phase I-IV trials.Responsible for the quality and timeliness of assigned statistical deliverables.As Lead Statistical Programmer, primarily responsible for all statistical programming activities on assigned studies including planning and coordination of activities for assigned statistical programming team members.Active participation in improvements to departmental processes and procedures.Provide mentoring within the Statistical Programming team.This position is perfect for you if you have:BSc/BA or equivalent in computer science, mathematics, statistics, life sciences or related field(s).Excellent SAS programming skills (BASE, MACRO, GRAPH).Excellent knowledge of CDISC standards.Statistical Programming experience within a CRO Pharmaceutical/Healthcare/Biotechnology industries.Experience in statistical programming initiatives, and development of processes.Knowledge and experience in database design and structures.The ability to perform all duties as a statistical programming project team member with no supervision. The ability to perform all duties of Lead Statistical Programmer on several concurrent studies with minimal supervision.Expert knowledge of clinical trial practices, procedures and methodologies.Strong oral and written communication skills.Excellent organizational/time management skills.An excellent investigative and meticulous approach to all activities and tasks.What we offer:Opportunity to be part of an innovative organization and work with exciting technologies.Mentoring and training to develop your skills in the clinical trials industry.The chance to be part of an effective, friendly and supportive team.Competitive employment package. For more information on Aixial Group Recruitment and consideration for other opportunities, please review the recruitment statement on our careers page - be aware that we do not accept resumes from outside agencies or recruiters unless specifically requested by a Aixial Group HR or Talent Acquisition Manager. Unsolicited agency or recruiter resumes will not be eligible for referral fees and will be considered candidates Aixial may directly contact for employment application.