Statistical Programmer: CDISC/SAS for Submissions

Katalyst CRO; Tampa (FL); On-site; USD 85,000 - 120,000; Part time

Job summary

A clinical research organization is seeking a skilled Statistical Programmer to manage and analyze clinical trial data. In this role, you will develop SAS programs, guarantee quality of statistical outputs, and support regulatory submissions. The ideal candidate holds a Bachelor's degree in a scientific discipline and has experience with SAS. You will work in a mid-senior level position that offers a contract employment type, collaborating with a team to ensure the highest quality of analysis and compliance with standards.

Qualifications

• Bachelor's degree or higher in a relevant discipline.
• Good experience in SAS and proficient in Macro Facility.
• Ability to work with CDISC standards.

Responsibilities

• Develop SAS programs for clinical trial data management.
• Contribute to regulatory submissions and data analysis.
• Ensure quality of statistical outputs prepared by providers.

Skills

SAS programming

Data analysis

Communication skills

Problem-solving skills

Teamwork

Education

Bachelor's degree in Statistics, Mathematics, Computer Science, or related field

Tools

SAS

Job description

A clinical research organization is seeking a skilled Statistical Programmer to manage and analyze clinical trial data. In this role, you will develop SAS programs, guarantee quality of statistical outputs, and support regulatory submissions. The ideal candidate holds a Bachelor's degree in a scientific discipline and has experience with SAS. You will work in a mid-senior level position that offers a contract employment type, collaborating with a team to ensure the highest quality of analysis and compliance with standards.