Position Details
About this role
Senior statistical programming lead responsible for developing analysis and reporting standards for BARDS across drug/vaccine projects.
Key Responsibilities
- Develop and validate global programming standards for ADaM datasets
- Develop and validate global programming standards for efficacy analysis and reporting
- Design and develop complex programming algorithms
- Provide technical consultation and analytical support
- Represent company on industry initiatives (R Consortium, TransCelerate, PHUSE, CDISC)
Technical Overview
Extensive SAS programming in clinical trials with SDTM/ADaM; experience with Unix/Linux; R and Python; XML; global programming standards.
Ideal Candidate
The ideal candidate is an experienced Associate Principal Scientist with 7+ years SAS programming in clinical trials, solid knowledge of CDISC SDTM and ADaM, and ability to develop global programming standards; proficient in R, Python and XML; able to collaborate across stakeholders in BARDS.
Must-Have Skills
Nice-to-Have Skills
Required Skills
Hard Skills
Soft Skills
Industry & Role
Clearance & Visa
Keywords for Your Resume
Deal Breakers
Lack of SAS programming experience in clinical trials, Lack of CDISC SDTM/ADaM knowledge, Inability to work in a hybrid model
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