Statistical Programmer

Role & responsibilities:

Equivalent combination of education, training, and relevant experience may be considered in place of the education and experience stated

Functional Knowledge:

Business Expertise:

Leadership:

Problem Solving:

Impact:

Interpersonal Skills:

What You Will Be Doing:

• Developing, validating, and maintaining complex statistical programs (SAS, R, or similar) for data manipulation, analysis, and reporting in clinical trials.
• Collaborating with biostatisticians and cross-functional teams to interpret study requirements and ensure the accurate implementation of statistical analyses.
• Preparing and reviewing statistical analysis plans (SAPs), programming specifications, and derived datasets to meet regulatory standards.
• Ensuring data integrity and compliance with industry regulations, including ICH/GCP guidelines, throughout the programming process.
• Mentoring junior programmers and assisting in training team members on programming techniques and best practices.

Preferred candidate profile

• Bachelors degree in statistics, mathematics, computer science, or a related field; advanced degree is a plus.

• 5+ years' experience

  as a statistical programmer within the clinical research industry, with strong knowledge of statistical methodologies and programming.

• Proficiency in programming languages such as SAS, R, or Python, with experience in clinical data management systems.

• Strong analytical and problem-solving skills, with a keen attention to detail and the ability to work independently.
• Excellent communication skills, with the ability to convey complex statistical concepts to non-technical stakeholders and collaborate effectively with team members.