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Dear Allstat Please find below one of our latest permanent Statistical Programming vacancy: Please contact me for further details on +44 207 6334825 A leading pharmaceutical company has an opportunity for an Experienced Principal Statistical Programmer to join there growing team. You would be based in there head office in Switzerland. PURPOSE OF ROLE The successful candidate will act as an Indication or Program Programmer for assigned project and will take a programming leadership role on the indication/project team. She/he will be responsible for the following activities: * Coordinate programming activities across several trials and indications with a given compound including publication and regulatory submission activities. * Lead the indication/project team including resources planning and coordination of the different programming sites internationally * Make certain that indication/project documents and specifications are consistent and comply with company standards by providing input into Study protocol, CRF and Data structures and outputs (listings, tables and figures) for phase I-IV clinical trials and submission activities. * Develop programming specifications for analysis datasets, pooled datasets and deliverables in consultation with the statistician. * Develop and comply with project/study programming standards and specifications following internal guidelines. * Support quality control and quality audit of deliverables. * Participate as required at all meetings, discussions and activities covering aspects of Statistical Reporting on trial/project level activities. * Track clinical trial milestones for statistical reporting deliverables. * Maintain records for all assigned projects and archiving of indication/project analysis and associated documentation. * Maintain efficient interfaces with internal and external customers and communicate effectively across line functions. * Program according to specifications, analysis datasets, pooled datasets, listings, tables and figures for phase I-IV clinical trials Qualifications * Bachelor/Master's degree in Mathematics, Statistics, Data Analysis Program or Computer Science (or equivalent degree with experience). * Ability to lead and coordinate programming work across several studies. * Industry experience is a must, using SAS in the analysis and the reporting of pharmaceutical data * Working knowledge and expertise with SAS (including SAS macro language) * Strong analytical skills and the ability to think laterally * Working knowledge of database design/structures * Good understanding of global clinical trial practices, procedures and methodologies. * Good understanding of regulatory requirements (e.g. GCP, ICH) * Fluent English (oral and written) Kind regards, Laura Laura Christie Senior Consultant, Biometrics, Europe Recruiting experts in Pharma HAYS Recruiting experts worldwide 25-27 Wootton Street London SE1 8TG T: +44 207 633 4825 F: +44 207 922 7101 E: [log in to unmask] hayspharma.com ------------------------------------------------ ****************************************************************************** This message (including any attachments) is confidential and may be legally privileged. If you are not the intended recipient, you should not disclose, copy or use any part of it - please delete all copies immediately and notify the Hays Pharma Helpdesk at [log in to unmask] . Any information, statements or opinions contained in this message (including any attachments) are given by the author. They are not given on behalf of Hays Pharma unless subsequently confirmed by an individual other than the author who is duly authorised to represent Hays Pharma. Hays Pharma is a member of the Hays Plc group of companies. Hays Plc is registered in England and Wales, number 2150950. Registered office, 250 Euston Road, London, England, NW1 2AF. ****************************************************************************** You may leave the list at any time by sending the command SIGNOFF allstat to [log in to unmask], leaving the subject line blank.