Labcorp Drug Development Job - 40831501 | CareerArc
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Company: Labcorp Drug Development
Location: Maidenhead, United Kingdom
Career Level: Mid-Senior Level
Industries: Healthcare, Pharmaceutical, Biotech


Job Overview:

  • Senior Statistical Programmer required to work for Labcorp Drug Development as a Lead Statistical Programmer
  • You will be employed by Labcorp Drug Development working in our Clinical Development Services division working across multiple Sponsors in a dedicated team that works purely on Phase I and IIa patient oncology studies
  • Home based anywhere in Europe or South Africa
  • You must have previous experience of working as a Lead Statistical Programmer within clinical trials using SAS
  • Oncology experience desirable but not essential
  • Candidates must be fluent in English language (both verbal and written)

Join our growing team and discover your extraordinary potential by working as a Labcorp Drug Development Senior Statistical Programmer within our Global Clinical Development Statistical Programming department.  Within this department there is a team that works solely on Phase I and IIa patient oncology studies across multiple Sponsors.  The position offers a strong support network, flexible working solutions and the opportunity to progress your career.  If you are looking to strengthen your Lead expertise within a varied and dynamic environment, then this is a fantastic opportunity.  This is a permanent, full-time office or home-based role anywhere within Europe or South Africa.


Job Primary Functions

  • Act as a Lead Statistical Programmer for projects, and act as a Statistical Programming consultant to clients and internal customers.
  • Plan, execute and oversee all programming activities on a study, including but not limited to, resource estimation, working within budget, meeting timelines, maximizing quality, interaction with other departments and the client
  • Develop and review SAS programs and output for SDTMs, ADaMs and TFLs, including submission deliverables e.g. Define XML/PDFs, Reviewers Guides, Analysis Results Metadata (ARM).
  • Mentor less-experience programmers in the processes around SDTMs, ADaMs and TFLs ensuring adherence to department practices and processes
  • Present and share knowledge at department meetings
  • Proactive involvement with process improvements, investigating and implement new procedures / methods when necessary
  • Degree
  • You must have previous experience of working as a Lead Statistical Programmer on complex studies within clinical trials using SAS
  • Oncology experience desirable but not essential
  • An understanding of the fundamental principles of programming, program development and review
  • Broad knowledge of all CDISC requirements related to SDTM and ADaM, including define.xml,
  • Reviewer's Guide and submission standards
  • Positive attitude and willingness to learn and contribute in a team setting and communicate effectively within the team environment
  • Good organization skills and the ability to prioritize own work
  • Self motivation and ability to work independently
  • A cooperative and team-oriented approach
  • Candidates must be fluent in English language (both verbal and written)





For a confidential discussion about this opportunity, please phone Peter Lewis on +44 (0) 7917 710 602.   To apply, please click on the APPLY button. 



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