
Expert Statistical Programming Professional
2 days ago
Key Responsibilities:
The Senior Statistical Programmer leads statistical programming support for multiple clinical research projects using SAS, ensuring regulatory-compliant output. Primary duties include developing documentation, writing efficient code, staying updated on programming techniques, and mentoring staff.
Responsibilities:
- Leads statistical programming support for clinical research study projects or study teams, collaborating with cross-functional teams.
- Develops detailed programming documentation, annotations, and specifications adhering to Standard Operating Procedures.
- Writes well-documented, high-quality code, conducts code review, supports programming validation as needed.
- Maintains knowledge of current statistical programming techniques to ensure adoption of sound methodologies.
Essential Qualifications:
- A bachelor's degree in a scientific discipline plus 4 years' experience in Statistical programming as a CDISC/TLF Statistical programmer in the Pharmaceutical/CRO environment.
- In-depth understanding of GCP principles and regulatory standards (e.g. FDA, EMA, and ICH guidance) in Clinical Research.
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