Position Details
About this role
Senior role overseeing statistical programming activities in clinical trials, ensuring compliance with industry standards and regulatory requirements.
Key Responsibilities
- Lead statistical programming activities
- Ensure regulatory compliance
- Oversee electronic submissions
- Manage data standards
- Coordinate with clinical teams
Technical Overview
Expertise in SAS, CDISC standards (SDTM, ADaM), electronic submissions, and clinical data management within biotech/pharmaceutical environments.
Ideal Candidate
The ideal candidate is a senior statistical programmer with over 12 years of experience in clinical data analysis, proficient in SAS, CDISC standards, and electronic submissions, with leadership capabilities.
Must-Have Skills
Nice-to-Have Skills
Tools & Platforms
Required Skills
Hard Skills
Soft Skills
Industry & Role
Keywords for Your Resume
Deal Breakers
Lack of SAS experience, No experience with CDISC standards, Must be authorized to work in the US
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