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Dear Allstat, Please find below details of our latest job posting for our client a leading Pharmaceutical Company. Senior Statistical Programmer Location: South East Role Working directly with the trial and project statistician and proactively with the Clinical Trial and Project teams, providing programming support. Implementing and supporting a harmonized approach to programming. Responsibilities Supporting the clinical research development process by providing statistical programming for new indications, substances and marketing claims. The ability to function as a Project Programmer or as the Trial Programmer focusing on complex trials that represent new challenges for which project and therapeutical knowledge is not given. Also the ability to supervise CRO’s working within the the statistical programming area on trial level. Skills Knowledge in database structures, set-up and medical terminology. Excellent working knowledge of all aspects of the SAS programming language used in Clinical trials programming and working knowledge of statistical concepts in support of analyses and reporting of Clinical trials. Must be precise, detailed oriented and able to understand data displays and their relationships. Possess good organisational, problem-solving and time management skills. Have the ability to prioritise work assignments and have the ability to work independently or as part of a team Good written English language and oral communication skills. Education / Qualifications A degree or relevant experience in a Mathematical, Computing or Life Science discipline. For more information on this role, please forward your CV details to [log in to unmask] You may leave the list at any time by sending the command SIGNOFF allstat to [log in to unmask], leaving the subject line blank.