Senior Statistical Programmer

  • Lisboa
  • Tfs Healthscience
TFS HealthScience is excited to be expanding our Strategic Resourcing Solutions (SRS) team and we are looking for an experienced, highly motivated Senior Statistical Programmer who shares our vision of providing clinical research excellence. Our Biometric team is a highly experienced international group of professionals led by an industry expert. We are a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. We combine the full-service capabilities and global reach of a large CRO with the flexibility and personal approach only a mid-size CRO can deliver. Our core values of Trust, Quality, Flexibility and Passion are what make TFS Healthscience the successful company it is today. Our values shape our culture and work ethic. They reflect what we stand for and guide our organisation. Together we make a difference. TFS HealthScience is looking for a Senior Statistical Programmer home based in any of the TFS HealthScience locations in Europe. The Senior Programmer is part of the Global Biometrics Department within Clinical Development and will work independently on preparing, conducting and completing programming tasks (mainly in SAS ) in assigned Study Teams according to company policies, SOP’s and regulatory requirements. We look forward to receiving your application soon! What can we offer you? A great place to work where you will get the chance to push your career to the next level, a global environment with global opportunities. You will also get the opportunity to be part of a team with highly intelligent, passionate experts from all over the world. TFS is a place for inspiration where we focus on the patients, saving lives and aiming to increase their quality of life by supporting our clients. Responsibilities Responsible for programming activities within assigned studies Programming to produce: Consistency checks/Data checks Listings Summary tables Graphics Statistical tests (if background in Statistics) Give input to the data validation plan Support e.g. the biostatistician, the clinical data manager and the safety manager with tables, listings, data transfer and statistical tests Program validation and documentation Development of general macros and applications to support other biostatistics programmers or end users Program/validate SDTM datasets incl. define.XML and SDTM reviewer’s guide Program/validate ADaM datasets and TFLs incl. define.XML and ADaM reviewer’s guide Write system and user manuals Actively contribute to the organization and development of routines to enhance the work at TFS Support in implementation/validation/improvement of new or existing software Coach, support and mentor of (new) employees Provide input into proposals which include programming (DM or statistics) Requirements Bachelor’s Degree, preferably in computer science, statistics or equivalent Minimum 5 years of relevant programming experience (preferably in SAS) in clinical data Good verbal and communication skills