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Dear Allstat, SEC Pharma is exclusively recruiting for 16 positions at various levels for a leading clinical trials company in Eastern Europe. Positions on offer are within Biostatistics and Statistical Programming as follows: Biostatistician/Principal Biostatistician: As a Biostatistician you will be involved in: · The production of statistical reports and statistical sections of integrated clinical reports. · The programming of tables, listings and figures. · Performing statistical analyses. · Communicating process improvement ideas within the department As a Principal Biostatistician, you will work independently as a Statistical expert and be involved in: · The successful delivery of project deliverables, on time with high quality. · Provide direction to other members of Biostatistics department and mentor more junior staff. · Provide broad statistical support, including trial design, protocol and CRF development on specific studies · Lead production and quality control of randomization, analysis plans, statistical reports, statistical sections of integrated clinical reports and other process supporting documents. · Perform sample-size calculations, generate randomization lists and write statistical methodology sections for inclusion in study protocols · Review publications and clinical study reports. · Provide statistical input into Data Monitoring Committee. · Understanding the regulatory requirements related to the specific therapeutic areas and the implications for statistical processing and analysis. · Interact with clients and regulatory authorities. Interested applicants should be degree educated in a Statistics discipline, with proven experience of working with clinical trials data within the Pharmaceutical industry. You should also have experience in SAS Programming, be able to work independently and have good business awareness. Statistical Programmer/Principal Statistical Programmer: As a Statistical Programmer you will be involved in: · Providing technical expertise for the conduct of clinical trials, and working with minimal supervision to support various programming activities related to the analysis and reporting of clinical study data. · Ensuring quality control on all process and technical activities related to derived dataset, table, listing, and figure programming in accordance with quality standards · Assisting in the coordination of project start-up activities. · Assisting in the production and QC of derived dataset specifications, programming specifications, and other process supporting documents. · Using efficient programming techniques to produce derived datasets, tables, figures and data listings. · Maintaining supporting documentation for studies. As a Principal Statistical Programmer you will be involved in: · Acting as an internal subject matter expert in specific areas providing technical support and expert advice. · Working independently to support various programming activities related to clinical systems, and/or analysis and reporting. · Coordinating project start-up activities. · Assisting in the production and QC of analysis plans, TLF mock-shell development, derived dataset specifications, programming specifications, and other process supporting documents. · Using efficient programming techniques to produce and/or QC derived datasets tables, figures and data listings. · Regulatory requirements concerning industry technical standards (CDISC). · Providing input into monthly forecasts and monitor the completion of forecasted units. · Creating standard macros and applications to improve the efficiency of the department. Interested applicants should be degree educated in a Scientific/Mathematics/Computer Science discipline with proven experience of working as a Statistical Programmer within the Pharmaceutical industry. You will have Experience in SAS and Experience working with systems used within the Clinical Trial process. Full job descriptions can be provided on request, salaries on offer are negotiable and competitive and can be discussed upon application. For further information, please contact Priya Mukherjee on +44(0)207 255 6665 or email: [log in to unmask]<mailto:[log in to unmask]> I look forward to hearing from you. Best regards, Priya Priya Mukherjee Principal Consultant Tel: +44 (0)20 7255 6655 Fax: +44 (0)20 7255 6656 Mobile: +44 (0)7717578256 Email: [log in to unmask]<mailto:[log in to unmask]> Web: www.secrecruitment.com 3rd Floor, Woolverstone House, 61-62 Berners Street London W1T 3NJ United Kingdom P Please consider the environment before printing this mail note ________________________________ 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. 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