• Lead all of Immunovant’s development programs • Provide clinical scientific leadership for the clinical development organization • Provide medical leadership for cross-functional internal workstreams including pharmacovigilance, biostatistics, clinical operations, regulatory affairs, etc. • Provide medical safety oversight for Immunovant’s development programs • Collaborate with partners in the pharmacovigilance department in the analysis of clinical trial safety data • Collaborate closely with partners in Clinical Operations and be accountable for clinical trial conduct and timelines for associated key deliverables • Lead the design and writing of clinical protocols and associated clinical documents • Lead the writing of clinical and safety sections of key Program documents including Investigational New Drug submissions, Investigator Brochures, Clinical Study Reports, Development Safety Update Reports, Biologics License Applications, and other regulatory submissions and responses • Be responsible for the preparation, analysis, and presentation of safety data to internal and external safety monitoring boards • Assume primary responsibility for presentations related to clinical trial data and assist in the preparation of meeting abstracts, posters, and presentations related to clinical trial data • Contribute to the writing of manuscripts and publications • Comply with Immunovant’s SOPs and adhere to ICH, GCP, and relevant regulatory guidelines • Provide medical leadership for internal audits and regulatory inspections • Assist in preparation of materials for Advisory Board meetings, IMVT BOD meetings, etc. • Develop and maintain strong, collaborative relationships with the broader Immunovant organization • Represent Immunovant externally and build successful relationships with multiple stakeholders including trial site Investigators, KOLs, and others