Lead Programmer

Jobtailor; Warszawa; On-site; PLN 90,000 - 120,000; Full time

Job summary

Jobtailor is seeking a Statistical Programmer to lead programming tasks for clinical trial data, focusing on quality, validation, and regulatory-ready reports. You will develop and validate analysis programs in R and SAS, collaborating with biostatisticians to apply robust methods.

The role emphasizes quality control, effective communication, and contribution to continuous process improvements within a regulatory-driven environment.

Qualifications

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

Responsibilities

• Lead statistical programming tasks with a focus on quality and continuous improvement.
• Develop and validate programs for statistical analysis and reporting of clinical trial data using R and SAS.
• Collaborate with biostatisticians to define analysis plans and methods to be applied to clinical data.
• Perform quality control checks on outputs to ensure accuracy in reporting.
• Assist in preparing statistical reports, presentations, and regulatory submissions.

Skills

Statistical Programming

R Programming

SAS Programming

Statistical Analysis

Data Validation

Analytical Skills

Problem-Solving Skills

Attention to Detail

Communication Skills

Team Collaboration

Education

Bachelor's degree in statistics, mathematics, or related field

Tools

SAS

R

Job description

• You will lead on statistical programming tasks requiring technical depth, with a focus on quality and continuous improvement.


• Developing and validating programs for statistical analysis and reporting of clinical trial data, using R and SAS.


• Collaborating with biostatisticians to define analysis plans and statistical methods to be applied to clinical data.


• Performing quality control checks on statistical outputs and ensuring accuracy and consistency in reporting.


• Assisting in the preparation of statistical reports, presentations, and publications for regulatory submissions.


• Contributing to process improvements by identifying efficiencies in programming practices and methodologies.

Requirements

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


• Experience in statistical programming, preferably in a clinical research or pharmaceutical setting


• Strong proficiency in SAS and R programming, with a solid understanding of statistical concepts and methodologies


• Excellent analytical and problem-solving skills, with a keen attention to detail


• Strong communication skills, with the ability to work collaboratively in a team environment and effectively convey complex information


• Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Core Competencies

Demonstrates expertise in statistical programming using R and SAS, with a strong focus on quality control and process improvement in clinical trial data analysis. Capable of collaborating effectively with biostatisticians and preparing comprehensive statistical reports for regulatory submissions.

Highest-signal resume keywords

• Statistical Programming


• R Programming


• SAS Programming


• Clinical Trial Data Analysis


• Quality Control

ATS Optimization Keywords

Hard Skills

• Statistical Programming


• R Programming


• SAS Programming


• Statistical Analysis


• Data Validation

Soft Skills

• Analytical Skills


• Problem-Solving Skills


• Attention to Detail


• Communication Skills


• Team Collaboration

Industry Keywords

• Clinical Research


• Pharmaceutical Setting


• Statistical Concepts


• Regulatory Submissions


• Process Improvement