Related skills
r sas cdisc sdtm oncology๐ Description
- Provide statistical leadership for oncology trials across Ph Ia00III.
- Lead SAPs, protocols, and CSRs.
- Design and review statistics for efficacy and safety analyses.
- Oversee SDTM/ADaM data and TLFs per CDISC.
- Support interim analyses, DMC activities, and adaptive designs.
- Collaborate with cross-functional teams; contribute to regulatory submissions.
๐ฏ Requirements
- PhD or MS in Statistics, Biostatistics, or related field.
- 8+ years (MS) or 6+ years biostatistics experience.
- Strong oncology clinical trials experience.
- Survival analysis, time-to-event endpoints, and complex designs.
- SAS and/or R proficiency.
- CDISC SDTM/ADaM knowledge.
- Regulatory submissions experience and health authority interactions.
- Immuno-oncology or hematology oncology experience (preferred).
๐ Benefits
- Professional development opportunities.
- Supportive culture and client-facing experience.
- Global CRO environment with cross-country teams.
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