Statistical Programmer

Katalyst Healthcares & Life Sciences

🇺🇸 United States

On-site

Manager or above

10 months ago

10 months ago

Not enough detail in this posting to match

Responsibilities:

The SAS/Statistical Programmer will also be responsible for ensuring the accuracy and consistency of clinical data.
The successful candidate will work closely with the Biostatisticians, Data Managers, and Clinical Research teams to develop and implement programming solutions to support clinical data analysis and reporting
Develop and validate SAS programs to support clinical trial data analysis and reporting
Create, maintain, and document SAS programming standards and procedures
Collaborate with Biostatisticians, Data Managers, and Clinical Research teams to ensure programming requirements are met
Perform data checks, quality control checks, and data review activities to ensure data accuracy and consistency
The SAS/Statistical Programmer will be responsible for providing programming support for clinical trials conducted within the pharmaceutical industry
Prepare datasets for analysis, including merging and cleaning data from various sources
Prepare and review tables, listings, and figures for clinical study reports
Ensure compliance with regulatory requirements and guidelines
Keep up to date with new SAS programming methods and software, as well as regulatory guidance

Requirements:

Bachelor's Degree in statistics, computer science, or a similar quantitative field
4+ years of clinical statistical programming experience within the pharmaceutical or related industry
Proficiency in SAS programming
Knowledge of CDISC data standards
Strong attention to detail and ability to work independently
Excellent problem-solving skills
Excellent verbal and written communication skills
Knowledge of regulatory requirements for clinical trials and drug development
Ability to work in a team environment and collaborate effectively with other stakeholders

Statistical Programmer · Katalyst Healthcares & Life Sciences