Labcorp Drug Development Job - 41386896 | CareerArc
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Company: Labcorp Drug Development
Location: Lisbon, Portugal
Career Level: Entry Level
Industries: Healthcare, Pharmaceutical, Biotech


Job Overview:

  • Biostatistician 2 required to work for Labcorp Drug Development supporting the Lead You will also have the opportunity to Lead some simple studies
  • Working in the Clinical Development Solutions business unit you will work with multiple Sponsors across several therapeutic areas in all phases of clinical trials
  • This is a permanent full-time role, either office based or home based anywhere in Europe or in South Africa
  • You must have previous experience of working as a Biostatistician in either a biotech, CRO or pharma company

Join our growing team and discover your extraordinary potential by working as a Labcorp Drug Development Biostatistician 2.  You will enjoy a varied role working for different sponsors across several therapeutic areas, supporting the lead on projects, leading some of your own simple studies and mentoring more junior members of the department.  The position offers an excellent support network with access to Labcorp Drug Development's statistical consultants, flexible working solutions and the opportunity to progress your career into a Senior role and beyond.


Job Primary Functions

  • Perform Lead Biostatistician role on simple studies, providing statistical oversight and attending relevant project meetings
  • Maintain awareness of project budgets and tasks, and effectively communicate the status of such tasks to line management and the project manager, as appropriate
  • Preparation of Statistical Analysis Plans (including mock TFL shells) for simple and medium complexity studies under the supervision of senior statistical staff
  • Perform statistical analysis for medium complexity studies
  • Conduct overall statistical review of TFLs for medium complexity studies prior to client
  • delivery
  • Review CRF and other study specific specifications and plans
  • May perform sample size calculation for Clinical Pharmacology studies under the supervision
  • of senior statistical staff
  • Provide statistical input and review of the CSR for simple studies
  • Generation and review of randomization schedules from provided specifications under the supervision of senior statistical staff
  • Master's degree, equivalent, or higher in Biostatistics or related field
  • You must have previous experience of working as a Biostatistician in either a biotech, CRO or pharma company
  • Ability to program in one or more statistical software packages (SAS®) used to conduct statistical analyses
  • Ability to effectively communicate statistical concepts
  • Interpersonal and effective communication skills
  • Cooperative and team-oriented
  • Self-motivation
  • The ability to work to tight deadlines while maintaining high standards
  • You must be fluent in English language (both verbal and written)




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



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