Senior Statistical Programmer – 12 Months – Berkshire
Biopharmaceutical, Clinical Research, Statistical Sciences, SAS Programming
Our client, a global biopharmaceutical leader, is looking to add to their highly skilled Statistical Sciences team in Berkshire with a contractor for 12 months. This company transform the lives of people living with severe diseases, particularly in the areas of the central nervous system and immunology. As the world moves towards tailored medicines and treatment, this organisation is at the forefront of translational medicine and target discovery.
As a Senior Statistical Programmer, you will join a talented team serving as a program or study-level programmer in a defined development program for the company mission.
*Supporting the programming and analysis of a clinical study within current or future UCB compounds or across multiple compounds/areas of research,
*Serving as a lead developer of new technologies, such as innovative visualization techniques or other non-traditional pharmaceutical programming.
*Leads and supports statistical programming activities for assigned clinical studies, submissions and development initiatives.
*Coordinating and provides input for assigned project and study teams on timelines and work product required to deliver high quality statistical programming services in close collaboration with CROs.
*Provides a high level of effective collaboration for statistical programming initiatives with key team members such as Data Operations, Medical Writing, Clinical Project Management, Marketing & Market Access
*May program, validate, maintain, and document statistical analysis programs for asset development on the basis of the SAP and of other documents
*Where applicable, develops innovative programming methodologies (i.e. interactive visualization, dashboards, etc.) to facilitate easier interpretation by customer base
*Ensures that submission and study datasets (SDTM and ADaM), tables, figures, listings, statistical output, and program documentation meet standards requirements of regulatory agencies
*Ensures that datasets, tables, figures, listings, and statistical outputs are produced in an efficient manner, following GSS procedures and standards. Develops specification documentation for datasets (SDTM and ADaM), pooled datasets, tables, figures, listings, and associated metadata.
We are looking for a talented programmer who has good experience in statistical programming support for the life cycle of a development compound (from phase I/II through phase IV and post approval activities). You should be able to performs as a competent and experienced statistical programmer by functioning as a technical resource, internal statistical programming consultant, and mentor to the statistical programming staff.
*Bachelor’s degree in statistics, programming, computer science or a related discipline.
*5+ years in statistical programming within the Biotechnology and/or Pharmaceutical Industry (including CRO’s).
*1+ year experience with statistical programming aspects required for regulatory submissions.
*Advanced SAS Software Programming skills, including experience with advanced DATA step, SQL and macro development to solve complex programming tasks.
*Good clinical studies design and analysis experience, including comprehensive understanding of drug development phases, clinical studies designs, efficacy endpoints and assessments and safety endpoints and assessments.
*Working knowledge of statistical principles, including descriptive and inferential statistical (parametric and non-parametric) methods and experience in using respective SAS procedures.
*Excellent written and verbal communication skills. Extensive experience in communicating with all levels of personnel across various departments, in domestic and international environments. Able to communicate complex quantitative ideas clearly.
*Excellent command of English, both verbal and written.
*Advanced knowledge of SDTM and ADaM programming requirements and practices.
*Able to work in a multicultural global environment
It would be great to hear from you if you are interested in a new challenge for the next 12 months. The hourly rate will be competitive and we will support you if you have not held a contract position before. Please contact Jade on +44 121 616 3472 for more information and an informal discussion.
Keywords: Biopharmaceutical, Clinical Research, Statistical Sciences, SAS Programming, Statistical Programmer, Berkshire, Slough
Paramount Recruitment Limited provides services as an agency and an employment business. We regularly have similar roles in this area. Please see our website for details or send your CV in to us to find out the latest opportunities.
Job Reference: JPSSP12_1537868911
Broadcast As: 184
Salary Currency: GBP
Salary per: Annum
Job Type: Full Time
Job Term: Permanent
Job Industry: Clinical Research
Job Specialism: Biometrics
Recruitment Consultant: Jade Page