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R statistical Programmer/Analyst

Remote: 
Full Remote
Experience: 
Mid-level (2-5 years)
Work from: 
Connecticut (USA), Illinois (USA)

Offer summary

Qualifications:

3-5 years of clinical trial development experience, Proficiency in R and SAS.

Key responsabilities:

  • Organize and analyze clinical trial data via R
  • Generate TLFs with focus on figures
  • Review and validate SDTM ADaM datasets
  • Utilize R Studio desktop app and R Shiny for data visualization
Katalyst HealthCares & Life Sciences logo
Katalyst HealthCares & Life Sciences Pharmaceuticals SME https://www.katalysthls.com/
51 - 200 Employees
See more Katalyst HealthCares & Life Sciences offers

Job description

Responsibilities and Requirements:
  • Organize clinical trial data (e.g., integrate EDC datasets to analyze data, generate descriptive summaries, etc.) via R.
  • Generate TLFs (emphasis on figures).
  • Review and validate SDTM & ADaM datasets has context menu.
  • Looking for an R statistical programmer/analyst (with SAS experience as well) to support a small biotech.
  • There is not a computing environment set up yet so the person will use the R Studio desktop app and leverage R (like R Shiny) for data visualization.
  • This role will require someone who is creative & resourceful in researching and "grabbing " R packages from the open-sources and at least 3-5 years of clinical trial development experience.

Required profile

Experience

Level of experience: Mid-level (2-5 years)
Industry :
Pharmaceuticals
Spoken language(s):
English
Check out the description to know which languages are mandatory.

Other Skills

  • Creativity
  • Resourcefulness

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