Programmer in Clinical Trials

Our approach to teaching will be a collaborative hands-on work with end-to-end dummy clinical data. You will gain necessary skills to create specifications, produce and validate datasets as well as produce simple and complex tables, listings and figures.

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Week 1,2 Week 3, 4 Week 5 Week 6,7
  • Introductions
  • ADaM specifications
  • ADaM* assignments
  • ADaM* source
  • ADaM* validation
  • TLFs* specifications
  • TLFs* assignments
  • TLFs* source
  • TLFs* validation
Week 8
  • Presentation
  • End of Training
Acronyms:
ADaM = Analysis Data Model
TLF = Tables, Listings, Figures

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  • BS. in Bioinformatics, Biotechnology, Biostatistics, Data Science or any analytical background.
  • Minimum knowledge about SAS or R programming and willingness to put effort into learning new skills.
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TRAINER

IULIANA CONSTANTIN
IULIANA CONSTANTINFounder
Iuliana Constantin has over 15 years of extensive SAS programming experience in solving non-routine situations in the pharmaceutical, diagnostic and device industry. She is passionate about sharing her knowledge gained in the industry with the new generation of leaders in the industry.

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Become a Professional in Clinical Trials Industry.