Position Details
About this role
This senior role involves leading statistical programming activities for clinical trials, ensuring compliance with data standards, and managing vendor relationships to produce submission-ready data outputs.
Key Responsibilities
- Lead statistical programming activities
- Oversee vendor deliverables
- Ensure compliance with data standards
- Develop analysis datasets and specifications
- Support electronic submissions
Technical Overview
Expertise in SAS, define.xml, electronic submission components, and clinical data standards, with leadership experience in managing programming teams and vendor oversight.
Ideal Candidate
The ideal candidate is a senior statistical programmer with 5+ years of experience leading programming activities in clinical trials, proficient in SAS and data standards, capable of overseeing vendor deliverables and ensuring high-quality submission-ready outputs.
Must-Have Skills
Nice-to-Have Skills
Tools & Platforms
Required Skills
Hard Skills
Soft Skills
Industry & Role
Keywords for Your Resume
Deal Breakers
Less than 5 years of relevant experience, Lack of experience with SAS or define.xml, No leadership experience in programming teams, Inability to work remotely in the US
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