Sr Statistical Programmer - 216792

Medix™; Seattle (WA); On-site; USD 85,239 - 121,401; Full time

Job summary

A biotech consulting firm in Seattle is looking for a Senior Statistical Programmer to support clinical research trials. Candidates should have over 5 years of experience in statistical programming and be proficient in SAS, R, or Python. Responsibilities include developing statistical programs, conducting quality control checks, and leading data analysis projects. This is a 6+ month contract paying $75/hr.

Qualifications

• 5+ years of experience in statistical programming for clinical research trials.
• Proficiency in programming languages such as SAS, R, or Python.

Responsibilities

• Develop and validate complex statistical programs.
• Conduct quality control checks on datasets and analysis outputs.
• Optimize programming processes and methodologies.
• Lead complex data analysis projects.
• Document programming activities and maintain version control.
• Provide technical guidance and mentorship to junior programmers.

Skills

Statistical programming

Quality control

Problem-solving

Communication

Education

Bachelor’s degree in Statistics, Biostatistics, Computer Science, or a related field

Tools

SAS

R

Python

Job description

We are looking for a Sr Statistical Programmer to support a biotech client of ours in Seattle, WA. Interested candidates must have 5+ years of experience in statistical programming for clinical research trials.

Details:

• 6+ month contract
• Pay: $75hr OBO

Overview

The Senior Statistical Programmer provides advanced programming support and leads complex data analysis projects. This role develops and validates statistical programs, conducts quality control checks on data and analysis outputs, and optimizes programming processes and methodologies to ensure accuracy, efficiency, and compliance.

Responsibilities

• Develop and validate complex statistical programs.
• Conduct quality control checks on datasets and analysis outputs.
• Optimize programming processes and methodologies to improve efficiency.
• Lead complex data analysis projects, collaborating with statisticians and data managers to ensure accuracy.
• Document programming activities and maintain version control.
• Provide technical guidance and mentorship to junior programmers.
• Ensure compliance with regulatory requirements and industry standards.
• Troubleshoot and resolve programming issues.

Required Qualifications

• Bachelor’s degree in Statistics, Biostatistics, Computer Science, or a related field.
• 4+ years of experience in statistical programming.
• Proficiency in SAS, R, or Python.

Preferred Qualifications

• Experience in clinical trials or research studies.
• Knowledge of CDISC standards (SDTM, ADaM).

Knowledge, Skills, and Abilities

• Strong programming and problem-solving skills.
• Attention to detail and ability to perform rigorous quality checks.
• Effective communication and collaboration skills to work cross-functionally.
• Ability to lead projects and provide mentorship.