Jobs at Immunovant

Lead CMC Quality Assurance for sterile drug product manufacture and clinical packaging. Provide GMP/GxP oversight of CDMOs/CMOs, approve batch records, support process control strategy, data integrity, batch disposition, inspection readiness, regulatory filings, and continuous improvement using eQMS and quality systems to ensure compliance and patient safety.

Lead biostatistics for multiple development programs: define and execute statistical strategy, contribute to protocols, SAPs, regulatory submissions, ensure compliance, apply innovative methods, collaborate cross-functionally, and manage study biostatisticians.

Lead month-end clinical and R&D accruals, prepare journal entries and reconciliations, analyze variances, review contracts, maintain SOX controls, support audits, and collaborate with Clinical Operations, Manufacturing, FP&A, CROs, and vendors to ensure accurate R&D accounting and reporting.