Position Details
About this role
This role involves developing and validating statistical programs for clinical research, ensuring compliance with data standards, and supporting regulatory submissions.
Key Responsibilities
- Lead dataset development
- Validate statistical programs
- Ensure data standards compliance
- Collaborate with clinical teams
- Mentor junior programmers
Technical Overview
Utilizes SAS for programming, CDISC standards for data formatting, and tools like define.xml for documentation, with a focus on clinical trial datasets and outputs.
Ideal Candidate
The ideal candidate is a senior-level statistical programmer with extensive experience in SAS, clinical trial data, and CDISC standards. They should have strong leadership skills, experience with regulatory submissions, and the ability to collaborate across teams.
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, No regulatory submission experience, Inability to work remotely, Less than 3 years of relevant experience
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