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SENIOR/PRINCIPAL STATISTICIAN PERMANENT- UK Location: UK- South East, commutable from London and Home Counties Start date: Anyone with up to a 3 month notice period Department: Statistical Sciences Salary: Basic Salary + Benefits + Bonus + homeworking Role This new position is with one of the world's leading Pharmaceutical companies leading the industry across multiple fields, working within one of the biggest and influential Statistics departments around. This position is open to Senior and Principal statisticians, those looking for a promotion or looking for challenging yet rewarding place to work. Along with the hugely experienced team and department and the prestige of working for a top 10 Pharmaceutical company comes a great culture behind the company consisting of great benefits including homeworking, bonus schemes, stock options and more. Responsibilities: These will include: - The writing of statistical methodology sections of individual protocols and formal Statistical Analysis Plans. - Performing statistical analyses of data and interpreting results to ensure validity. - Interacting with Data Management personnel as necessary to ensure that datasets are in usable format. - Ensuring that appropriate analysis programs are developed for current clinical studies. - Interacting with Medical Writers in the production of statistical and integrated clinical/statistical reports and other documents containing statistical information, including draft documents. - Maintaining the highest standards of quality across all statistical work performed - Interacting with other departments, such as Clinical Operations and Project Management, to ensure a high level of client satisfaction through the successful execution of projects. - Mentoring and supporting other members of the Biostatistics team and providing statistical expertise to other functions - Contributing towards the development of client presentations and information sources. Education/Qualifications: - MSc degree or Ph.D. in statistics based subject with previous experience of working on clinical trials within pharmaceutical development or academic research. - Proficient in the use of SAS and demonstrated ability to perform statistical analyses of clinical data. - Ability to work in a fast-paced, team-oriented environment. - Strong attention to detail and quality control - Proven organisational and planning skills and capability to work to challenging timelines - Ability to read, analyse, and interpret common scientific and technical journals. - Thorough knowledge of applicable regulatory rules and guidelines, e.g. ICH Guidelines. If this position is of interest to you and would like a more detailed job specification please send an updated CV to [log in to unmask]<mailto:[log in to unmask]> or alternatively call me on +44 (0) 203 465 0040 for a confidential discussion. Kind Regards, Ricardo Ricardo Lucas Resourcer, Statistics & SAS Recruiting experts in Life Sciences HAYS Recruiting experts worldwide Hays Specialist Recruitment 4th Floor 107 Cheapside London EC2V 6DB T: +44 203 465 0040 E: [log in to unmask]<mailto:[log in to unmask]> hays.co.uk Refer a friend to Hays<http://www.hays.co.uk/refer-a-friend/> and receive vouchers as a reward when we place them in a new role. ********************************************************************* 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. To update your contact details or relevant information, please contact the sender. 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