Sr. Statistical Programmer - UK/EU (CP06HM731)
Horsham, England, United Kingdom
5d ago

Why Cmed?

Cmed occupies a unique position in the clinical research industry, not only as an expert in the operational delivery of clinical trials but also as a developer of its own technologies for managing clinical data.

Cmed’s core CRO speciality areas include Full Service Solutions for immuno-oncology and cell & gene therapy; and Data Science and Analytics services.

This is a very exciting time to join Cmed, as we start to leverage our already considerable expertise in the delivery of clinical trials with encapsia™.

This unique combination of operational expertise and the latest technology, helps reduce the costs and increase the speed of developing new medicines, essential to both improving and saving the lives of patients.

The role

We are currently looking for an enthusiastic and talented Senior Statistical Programmer to be fully home-based from anywhere in the UK / EU.

Your core responsibilities :

  • Statistical programming for both production and QC of SDTM and ADaM datasets, TFLs, data listings, data summaries, figures and statistical appendices for global Phase I-IV trials.
  • Responsible for the quality and timeliness of statistical programming deliverables.
  • As programmer, to be primarily responsible for all statistical programming activities on allocated studies including planning and coordination of activities for assigned statistical programming team members.
  • Active participation in improvements to departmental processes and procedures.
  • 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 or minimum supervision.
  • 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 organisation 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.
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