Job Overview
We are seeking an experienced Statistical Programmer to join our team.
Responsibilities:
* Prepare clinical study reports for regulatory submissions.
* Develop and maintain CDISC datasets to ensure data quality and integrity.
Requirements:
* Minimum 2 years of experience in statistical programming.
* Demonstrated knowledge of CDISC standards and regulations.
Bonus Points:
* Familiarity with clinical trials and pharmaceutical industry.
* Strong analytical and problem-solving skills.
About the Role:
* This is a challenging opportunity for a skilled programmer to grow professionally.
* The ideal candidate will be highly motivated, detail-oriented, and able to work independently.