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About Summit:
- Biopharmaceutical oncology company advancing Phase 3 studies in NSCLC and CRC.
- Team driven by integrity, collaboration, and purposeful urgency.
Role:
- Prepare, publish, and QC eCTD regulatory submissions to health authorities.
- Maintain Veeva RIM records and support submission projects.
Requirements:
- Bachelor's in life sciences with 4+ years Regulatory Operations experience.
- Strong Word, Adobe Acrobat, eCTD, and FDA/ICH standards expertise.
Summit Therapeutics Inc.
Summit Therapeutics is a biopharmaceutical oncology company focused on improving quality of life and resolving serious unmet medical needs. Its global team is driven by core values of integrity, collaboration, and purposeful urgency, with multiple Phase 3 clinical studies in oncology.