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PHASTAR is a niche CRO focusing on statistics and clinical trial reporting. Established in 2007, PHASTAR have rapidly grown our team over the last eight years with average yearly growth of 49%. As demand for our services increase, we are looking to continue with expansion of our team and are recruiting for multiple positions across our offices in London, Manchester, Kent and our new Glasgow office. We currently have various vacancies available on a permanent or contract basis . Senior Statistician . Principal Statistician . Principal Programmer What we offer: . Advancement of your career in an intellectually-stimulating, dynamic, supportive environment . Variety of projects in statistical consultancy and clinical trial reporting (range of therapeutic areas and phases) . Excellent remuneration (competitive salary, pension, healthcare, conferences and courses etc.) Principal Statistician Job description: * Manipulate, summarise and analyse clinical trial data using a variety of statistical methods * Function as statistical expert across a number of studies * Preparation of study protocols and development of statistical analysis plans * Supervise work of less experienced Statisticians * Being a client contact for the Biostatistics team Requirements: * PhD or MSc in Biostatistics or related discipline * Experience working within a clinical trials environment (Pharma or CRO) * Previous experience working with SAS * Ability to communicate Statistical issues across multi-disciplinary team * Excellent written and verbal communication * Familiarity with GCP and ICH guidelines Senior Statistician Job Description * Manipulate, summarise and analyse clinical trial data using a variety of statistical methods, ultimately delivering clinical trial results to an agreed timeline with optimal quality * Project management responsibilities, including allocating staff, predicting and planning resources * Responsible for ensuring the team meets the highest quality standards, and follows the principles detailed in PHASTAR's internal procedures * Preparation and review of study documentation e.g. protocols and statistical analysis plans * Ability to advise, mentor and teach both internal and external statisticians with regards to statistical and data analysis methods * Act as a study expert for a number of studies, with an ability to clarify details on analysis methods for the internal PHASTAR team * Maintaining a positive and engaging client relationship with regards to statistical issues Candidate Requirements: * PhD or MSc in Biostatistics or related discipline * Experience working within a clinical trials environment (Pharma, CRO or academic) * Previous experience performing statistical analysis using SAS Principal Programmer Job Responsibilities: * Function as a programming expert across a number of studies * Support in the submission activities for the study * Maintaining a positive and engaging client relationship with regards to statistical and/or programming issues . Focusing on the eCRF development process . Ability to provide knowledge to solve any arising or complex problems Candidate Requirements: . Educated to degree level or equivalent . Previous experience of working at project lead level within the pharmaceutical industry . High level of proficiency in SAS and related software . Ability to communicate with various members of the team . Ability to use a broad range of tools including data capture, data extraction, UNIX scripting Please contact me for more information, if you are interested in applying of the role, please email me your CV to [log in to unmask] or call 020 7183 7061 Feel free to share this with your network if you know someone who may be interested. Kind Regards Meera Chauhan Talent Acquisition Specialist PHASTAR [log in to unmask] 020 7183 7061 www.phastar.co.uk You may leave the list at any time by sending the command SIGNOFF allstat to [log in to unmask], leaving the subject line blank.