Statistical Programmer Iii

2 semanas atrás

Lisboa, Portugal Cmed Tempo inteiro

AIXIAL Group is an international Contract Research Organization (CRO), a part of the ALTEN Group, providing complex services in clinical trials (phase I-IV) and non-interventional studies. Our offices are located in France, Belgium, Switzerland, Germany, Denmark, Sweden, UK, Romania, US, and Czech Republic.

The AIXIAL Group occupies a unique position in the clinical research industry, not only as an expert in the operational delivery of clinical trials for immuno-oncology and cell & gene therapies, but also as a developer of its own game-changing EDC and eSource platform encapsia for managing clinical data.

This is a very exciting time to join Statistical Programming as we are at the cutting edge, defining new and more efficient ways to design, capture, manage, review, and visualize clinical trial data and we are now looking for talented Statistical Programmer III.

This role can be remote anywhere in the UK or 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 Lead 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 supervision. The ability to perform all duties of Lead Statistical Programmer on several concurrent studies with mínimal 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 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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