The Principal Statistical Programmer, Standards will support the development and maintenance of clinical data standards for a prominent Pharma company. The role requires a high degree of self-motivation, attention to detail, and exceptional problem-solving skills. Previous experience with implementing CDISC standards is required.
Requirements
- Bachelor's degree in computer science, math, statistics, biology, pharmacology, or related.
- 8+ years' experience as a Statistical Programmer with recent experience working on a Global Standards team or have created Global Standards within a Sponsor or CRO environment
- Expert knowledge of SDTM and ADaM data standards and FDA/PMDA/EMA submission requirements required
Benefits
- IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law.
- IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.