Statistical Programmer

2 days left

Horsham, West Sussex (GB)
15 Apr 2021
15 May 2021
Full Time
Contract Type
Experience Level

Compass Life sciences are working with a Global Clinical Research Organisation who are currently actively recruiting for a number of positions.   
We are currently looking for an enthusiastic and talented Senior Statistical Programmer to be fully home-based.   
We are considering candidates across the UK and Europe   
As a CRO, our client is made up of highly talented experts from across the sector, focussed on clinical trials, and the data that comes from them.  They are a valued partner to many of the top Pharmaceutical and Biotechnology companies in the world, and they have built strong long-standing relationships based on repeated successful delivery of studies, using revolutionary ways of gathering, managing, and analysing data in clinical trials.       
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 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.
Please contact Gareth Hughes-Jones at or +44(0) 2392 316 034 for further information.        
Compass Associates Ltd. trading as Compass Life Sciences are acting as a Recruitment Consultancy for this permanent vacancy; we offer £250 worth of Amazon Vouchers for each successful recommendation.  

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