Statistical Programmer

Our client is a leading international CRO currntly opperating out of Europe and the US. The are well established and have a very exciting, unique approach to their clinical research.

Core Responsibilities:

• Statistical programming for both production and QC of derived datasets, data listings, data summaries, figures and statistical appendices for global Phase I-IV trials.
• Creation of study specifications for analysis datasets and pooled datasets for phase I-IV clinical trials.
• Responsible for the quality and timeliness of statistical programming deliverables.

Essential Work Experience and Qualifications:

• Minimum of BSc/BA or equivalent in computer science, mathematics, statistics, life sciences or related field(s).
• Good SAS programming skills (BASE, MACRO, GRAPH).
• Knowledge and experience in database design and structures.
• Minimum of 1 years experience in programming in a clinical trials environment or in a related field.
• Knowledge of clinical trial practices, procedures and methodologies.
• Basic knowledge of statistical principals underlying clinical trials.

Key Words: SAS Programmer BASE MACRO GRAPH design structure Statistics Perm Surry