Senior Statistical Programmer Lead (R & SAS)

ICON Strategic Solutions

Warszawa

On-site

PLN 180,000 - 300,000

Full time

14 days+

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Benefits offered by this job

Annual leave
Health insurance
Retirement plan
Employee assistance program
Life assurance

Job summary

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re excited to welcome a Senior Statistical Programmer I to join our team in shaping the future of clinical development.

You will lead statistical programming tasks, focusing on quality and continuous improvement, and collaborate with statisticians on analysis plans. You will develop and validate programs for statistical analyses and reporting of clinical trial data using SAS and R, ensuring accuracy and

Qualifications

  • Bachelor's degree in statistics, computer science, mathematics, or related discipline is required.
  • Experience in statistical programming, preferably in clinical research or pharmaceutical setting.
  • Strong proficiency in SAS and R programming.
  • Excellent analytical and problem-solving skills with attention to detail.
  • Strong communication skills and ability to work collaboratively in a team.

Responsibilities

  • Develop and validate programs for statistical analysis and reporting of clinical trial data using SAS and R.
  • Collaborate with biostatisticians to define analysis plans and methods.
  • Perform quality control checks on statistical outputs for accuracy and consistency.
  • Assist in preparing statistical reports, presentations, and publications for regulatory submissions.
  • Contribute to process improvements by identifying programming efficiencies.

Skills

SAS programming
R programming
Statistics
Data analysis
Communication

Education

Bachelor's degree in statistics, computer science, mathematics, or related discipline

Tools

SAS
R

Job description

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re excited to welcome a Senior Statistical Programmer I to join our team in shaping the future of clinical development.

You will lead statistical programming tasks, focusing on quality and continuous improvement, and collaborate with statisticians on analysis plans. You will develop and validate programs for statistical analyses and reporting of clinical trial data using SAS and R, ensuring accuracy and

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