Job Summary
A pharmaceutical research and consulting firm is in need of a Remote Senior Clinical Trial Statistical Programmer.
Core Responsibilities Include:
- Adhering to programming specifications and study specific requirements
- Planning, organizing and prioritizing workload
- Creating listing and safety outputs
Applicants must meet the following qualifications:
- Master’s Degree or Bachelor’s Degree with experience
- Proficiency in SAS programming and using SAS macros
- CDISC SDTM and ADaM dataset development and validation experience
- Proficient in Microsoft Office Suite
- Experience in supporting clinical research and trial for a CRO/Pharmaceutical/Biotech company