Clinical Data Programmer

138179
  • 45000 EUR - 60000 EUR
  • portugal, Portugal
  • Permanent

Main Responsibilities:

  • Collaborates with the Clinical Data Programming & Biostatistics Coordinator to develop the Department activity plan and budget, managing activities within the allocated budget.
  • Contributes to study design definition and develops the statistical section of CSPs or other regulatory documents.
  • Develops SAPs (Statistical Analysis Plans).
  • Conducts quality control of CDISC SDTM and ADaM Define.XMLs and Reviewer’s Guides from existing clinical study data.
  • Performs quality control on generated outputs and the statistics section of final clinical documents (e.g., CSPs, CRFs, SAPs, and CSRs).
  • Executes data analysis defined in SAPs, post-hoc analysis, and relevant exploratory analyses of clinical study data.

 

Requirements:

  • Proficient in written and spoken English and Portuguese (spoken, written, and read).
  • Strong statistical knowledge.
  • Proficient in developing Statistical Analysis Plans.
  • Bachelor's/master’s degree in bioinformatics, Computer Science, Statistics, or related areas.
  • Over 2 years of programming skills (SAS, R, Python, etc.).
  • Over 2 years of experience in generating CDISC SDTM and ADaM domain datasets, from clinical trials.

 

Do not miss out on this opening – apply below or contact Ryan Tanner at Meet or email directly to ryan.tanner@peoplewithchemistry.com

Ryan Tanner Division Manager

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