Related skills
r sas biostatistics clinical trials cdisc📋 Description
- Lead statistics for oncology trials across Phase I–III.
- Support regulatory submissions (IND/NDA/BLA) and CRO processes.
- Provide statistical leadership for client-facing CRO engagements.
- Develop SAPs, protocols, and CSRs; manage SDTM/ADaM datasets.
- Oversee analyses, DMC activities, and adaptive designs.
- Mentor junior statisticians; collaborate with cross-functional teams.
🎯 Requirements
- PhD or MS in Statistics, Biostatistics, or related field.
- 8+ years (MS) or 6+ years (PhD) biostatistics experience.
- Strong oncology clinical trial experience; IO/Heme preferred.
- Survival analysis, time-to-event endpoints, complex designs.
- Proficiency in SAS and/or R; CDISC SDTM/ADaM expertise.
- Experience with regulatory submissions and interactions.
- Ability to mentor junior statisticians and lead teams.
🎁 Benefits
- Remote work option with global client exposure.
- Strong mentoring and professional development.
- Client-facing role with cross-functional collaboration.
Meet JobCopilot: Your Personal AI Job Hunter
Automatically Apply to Data Jobs. Just set your
preferences and Job Copilot will do the rest — finding, filtering, and applying while you focus on what matters.
Help us maintain the quality of jobs posted on Empllo!
Is this position not a remote job?
Let us know!