Senior Clinical Data Programmer
Bloemfontein, Orange Free State, South Africa
13d ago
  • Review the respective study protocol / CRF
  • Review of database setups
  • Development of data import programs
  • Development of data validation programs
  • Development of mapping programs (CDISC, HL7, PAREXEL, Client)
  • Reconciliation of external data
  • Development of data listings (including clean file listings, Protocol deviation Listings, patient profiles, etc)
  • CDISC SDTM and define.xml programming
  • Creation of annotated CRFs
  • Adherence to defined / describe processes
  • DM QC as assigned
  • Provide technical support on projectsQualifications
  • Ability to work with cross-functional groups.
  • Ability to understand complex organizational relationships.
  • Good programming background and problem solving approach.
  • Good background and basic understanding of further statistical analysis processes.
  • Willingness to work overtime.
  • Detail-oriented with ability to work creatively and flexible in a fast-paced environment.
  • Good knowledge of PC or Unix SAS.
  • Demonstrate a sound awareness of all relevant regulations, including GCP.
  • Bachelor’s degree (or equivalent) in Mathematics, computer science or relevant discipline.
  • Good English knowledge.
  • At least 5 years experience in Database or Biostatistical programming in a clinical research environment is essential.
  • Experience in setup and / or programming in SAS or any EDC system is preferred.
  • Qualifications

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