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Dear Allstat, My client, a leading global Pharmaceutical company, is looking to recruit an Associate Director to work as a member of an international multi-disciplinary team of statisticians, statistical programmers, medical writers, data managers and project physicians. He/she will focus on the statistical support of clinical research and development of medicines for the Central Nervous System (CNS). The statistician will lead a local team of programmers and statisticians working on a project for the development of an analgesics compound. TASKS & RESPONSIBILITIES: The successful candidate will be responsible for the statistical support of Phase-1, Phase-2 and Phase-3 trials. This includes the design and analysis of trials, assistance in protocol writing, randomization, designing CRF, independent writing of statistical analysis plans, report writing and review, and statistical method development. He/she will take part in crossfunctional working groups and in meetings with the pharmaceutical regulatory authorities. The candidate will possess a thorough understanding of team needs and departmental standards, complete assignments accurately and timely, anticipate and recommend resolution for unexpected issues, and assist new statisticians with team deliverables. The candidate will provide information to statistical programmers, inform management of project status, perform coordination functions, enforce consistency within a project, enforce and maintain departmental standards, and provide recommendations to improve processes. The candidate will also provide statistical advice, practice sound statistical judgment, and recommend new statistical methods, as needed. SKILLS & EXPERIENCE: - MSc (including Belgian "Licentiaat) or PhD in statistics or biostatistics with in clinical drug development. - Good communication, presentation, organizational and problem-solving skills. - Ability to work independently and effectively in a team environment and to communicate with non-statisticians about statistical findings is necessary. - SAS experience is a must. Experience with S-PLUS and other statistics software is preferred. - Regulatory guidelines experience of ³ 4 years is required. - Leadership experience is required. - Experience in writing of statistical analysis plans, reports and other documents in English is a must. If you would like to discuss this position in detail, or for a confidential consultation on all of our current Biostatistics and Programming opportunities in the UK and Europe, please contact me directly. Details of our current contract and permanent vacancies can also be found at: http://www.jamesharvard.com/pharma/careers_browse.htm. I look forward to hearing from you. Kind Regards, Martin Martin Grindrod Consultant ~ Biostatistics Division James Harvard Pharmaceutical Ltd T. 020 7922 7128 M. 07884 001 300 F. 020 7922 7101 E: [log in to unmask] W: www.jamesharvardpharma.com 25 - 27 Wootton Street : Waterloo : London : SE1 8TG For all our latest Stats and Programming vacancies please visit our website www.jamesharvardpharma.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 James Harvard 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 James Harvard unless subsequently confirmed by an individual other than the author who is duly authorised to represent James Harvard. James Harvard is a member of the Hays Plc group of companies. Hays Plc is registered in England and Wales, number 2150950. Registered office, 141 Moorgate, London England, EC2M 6TX. ******************************************************************************