4 days ago
• Lead clinical operations oversight for Immunovant’s drug development lifecycle • Develop program strategies and ensure achievement of corporate targets • Manage CRO/vendor selection and oversee documentation • Ensure adherence to regulatory requirements and improve processes • Oversee clinical protocols, study manuals, and other key documents • Participate in continuous improvement initiatives for cost-reduction and efficiency • Build relationships with internal stakeholders for clinical trial execution • Manage clinical operations team with performance reviews and staff development • Collaborate across functions for clinical operations and project management
• Bachelors in Life Sciences with an advanced degree preferred • At least 15 years of experience in the pharmaceutical industry, with at least 10 years in a clinical leadership role on a cross-functional drug development project team • PMP is a strong plus • Global experience working across all phases of clinical research (Phases 1-4) • Working knowledge of ICH and GCP regulations is required • Experience selecting and oversight of CROs/vendors required • Experience in rare disease therapeutic areas and patient engagement strategies preferred • Direct supervisory experience • Unrelenting dedication to delivering quality results • Integrity, in word and action • Willingness to roll up your sleeves to get the job done
• Unlimited paid time off • Parental leave • Full range of medical, dental, vision, 401k, and other benefits
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