Dear Allstat,
Please see below our latest vacancy.
Manager Statistical Programming - CRO - UK
Core Responsibilities:
• Line management of a team of Statistical and /or SAS Programmers.
• 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.
• As a member of the management team within the function provide input to the strategic direction of the group and support the implementation of this.
• Program analysis datasets, pooled datasets, listings, summaries, figures and tables for phase I-IV clinical trials and for overall summaries of safety and efficacy.
• Production of study specifications for analysis datasets and pooled datasets for phase I-IV clinical trials.
As a Lead Statistical Programmer have overall statistical programming responsibility and accountability for the following on assigned studies:
Adherence to agreed timelines
Delivery of high quality products
Resource forecasting and keeping department resource tool up to date as agreed with Director Global Programming Ensuring proactive and timely communication with programming team, other functional leads and project / programme manager Financial management of statistical programming budget Ensure adherence to SOPs and any project or client specific standards or processes
Essential Work Experience and Qualifications
• Minimum of BSc/BA or equivalent in computer science, mathematics, statistics, life sciences or related field(s).
• Experienced line manager with proven success in this role
• Excellent SAS programming skills (BASE, MACRO, GRAPH).
• 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 multiple concurrently active studies with no supervision.
• Knowledge of clinical trial practices, procedures and methodologies.
• Basic knowledge of statistical principals underlying clinical trials.
If you have the skills and experience for this opportunity please email your C.V. to [log in to unmask] or call +44(0)1273 727 930 for further details.
Andrea is a Biometrics expert at Stelfox Pharmaceutical Search covering Europe, UK, North America and Asia.
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