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R Statistical Programmer Analyst

Remote: 
Full Remote
Contract: 
Full time
Experience: 
Mid-level (2-5 years)
Work from: 
New Jersey (USA), United States

Offer summary

Qualifications:

At least 3-5 years of clinical trial development experience, Experience with organizational skills for clinical trial data.

Key responsabilities:

  • Support a small biotech using RStudio for data visualization
  • Researching and utilizing R packages for analysis
  • Organize clinical trial data using R
  • Generate TLFs with emphasis on figures
  • Review and validate SDTM and ADaM datasets
Katalyst HealthCares & Life Sciences logo
Katalyst HealthCares & Life Sciences Pharmaceuticals SME https://www.katalysthls.com/
51 - 200 Employees
About Katalyst HealthCares & Life Sciences
Katalyst Healthcare's & Life Sciences (Katalyst HLS) is a Global Contract Research Organisation that provides End-to-End Clinical Research Services for Healthcare and Life Sciences companies globally. At Katalyst HLS offers ICH-GCP compliant clinical trial services from Phase I–IV in all key therapeutic areas to support clinical development and research requirements and also provides validation, quality and regulatory services for Pharma/Bio-Pharma/Medical Device industries. Services:- Clinical Trial Management- Clinical Data Management- Biostatistics & Statistical Programming- Medical Writing- Pharmacovigilance- Quality and Regulatory Affairs- GMP, GLP and GCP Validations- Manufacturing Process Validations- Equipments & Instruments Validations- Computer Systems Validations- Human Resourcing
See more Katalyst HealthCares & Life Sciences offers

Job description

Responsibilities:

  • Looking for an R statistical programmer/analyst to support a small biotech. There is not a computing environment set up yet so the person will use the RStudio 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.

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 .

Required profile

Experience

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

Hard Skills

Shiny (R Package)Clinical Trial PlanningR (Programming Language)RStudioData Visualization

Other Skills

  • Creativity
  • Resourcefulness
Are you interested?

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