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Ref: 275/11c Statistical Programmer Major Pharmaceutical Client - Mainland Europe £ Excellent Salary + Benefits Package For a confidential consultation call James Carrera on 0044 (0) 207 255 6665 or email your CV to [log in to unmask] Job Summary: The Statistical Programmer provides statistical software programming solutions and their documentation to support analyses and reporting of clinical trial data for regulatory submissions. Participate in the statistical programming team and gives support to the assigned clinical studies. The Statistical Programmer performs assigned statistical programming activities such that agreed objectives, standards, deadlines and other requirements with respect to specifications, program development, quality assurance and report delivery are attained in accordance with applicable processes. Accountabilities/Responsibilities: * Provide support to the statistical programming team on activities related to analysis and reporting of assigned drug development study data. * Perform trial protocol and Case Report Form (CRF) review. Create data structures definitions including CRF annotations for clinical trials. Ensure consistency and adherence to available standards. * Perform the user acceptance testing of data structure provided to PDIB by Data Management and execute data quality acceptance checks. Develop additional study-specific checks as required. * Interact with members of the statistics and statistical programming team to clarify requirements. * Contributes to programming specifications for analysis datasets (VADs), listings, tables, and figures under guidance of a senior team member. * Program, validate and document VADs, listings, tables, and figures for clinical trials according to the agreed specifications, with high quality and within agreed time lines. * Adhere to statistical programming standards, effectively use available standard programs, ensure availability of appropriate documentation and comply with Standard Operating Procedures. * Execute electronic submission process if applicable. * Support senior member of the statistical programming team in maintaining efficient interfaces with internal and external customers. * Support statistical programming group in implementing user aspects of improvement initiatives, especially with respect to statistical programming and technical implementations of data processing as well as analysis and reporting procedures. * Contribute to internal training related to statistical programming activities. Essential Skills & Capabilities: * University education or equivalent in Mathematics, Statistics, Computer Science or other analytical field. * At least 3 years of pharmaceutical industry drug development experience using SAS. * Good knowledge of SAS programming language, level of proficiency with SAS/Base, SAS Macro, SAS/Graph, SAS SQL and some SAS/STATS. * Good knowledge of English in a business environment. * Basic knowledge of drug development process in particular on collection, storing, processing and analysis of clinical trial data. * Knowledge and in Data base interfaces and programming experience in a UNIX operating system are considered a distinct advantage. For further details or a confidential conversation please contact me directly: James Carrera Statistics, Biostatistics & Programming Pharmaceutical, Healthcare & CRO Division Tel: +44 (0) 207 255 6665 [log in to unmask] http://uk.linkedin.com/in/jamescarrera Pharmaceutical, clinical trials, statistician, statistics, statistical, SAS, programmer, programming, statistics, statistician, biostatistics, biostatistician, medical affairs SEC Recruitment Ltd Company registered in England and Wales No. 5808613 - Registered Office: RDL House, 1 Chertsey Road, Woking, Surrey GU21 5AD. IMPORTANT NOTICE: The information in this e-mail and any attached files is CONFIDENTIAL and may be legally privileged or prohibited from disclosure and unauthorised use. The views of the author may not necessarily reflect those of the Company. It is intended solely for the addressee, or the employee or agent responsible for delivering such materials to the addressee. If you have received this message in error please return it to the sender then delete the email and destroy any copies of it. If you are not the intended recipient, any form of reproduction, dissemination, copying, disclosure, modification, distribution and/or publication or any action taken or omitted to be taken in reliance upon this message or its attachments is prohibited and may be unlawful. At present the integrity of e-mail across the Internet cannot be guaranteed and messages sent via this medium are potentially at risk. All liability is excluded to the extent permitted by law for any claims arising as a result of the use of this medium to transmit information by or to SEC Recruitment Limited. You may leave the list at any time by sending the command SIGNOFF allstat to [log in to unmask], leaving the subject line blank.