Dianthus Therapeutics is a clinical-stage biotechnology company based in New York City and Waltham, Mass. Focused on developing novel monoclonal antibodies with enhanced selectivity and potency, the company aims to create transformative medicines for severe autoimmune and inflammatory diseases. Led by an experienced team of biotech and pharma executives, Dianthus is pioneering next-generation antibody complement therapeutics.
Open Positions
Head of Global Medical Affairs
15+ years of biopharmaceutical experience, 8+ years of medical affairs leadership, and deep expertise in rare diseases and autoimmunology required
Regulatory Information Manager
2-3 years of experience in Pharma/Biotech industry, Bachelor's degree in Science, project management mindset
Director, Clinical Quality Assurance
12+ years of experience in GxP, BS or MS degree in life sciences or related field, 5+ years in GCP within the biotech or pharmaceutical industry
Senior Director, Clinical Vendor Procurement and Management
15+ years of experience in clinical procurement, strong RFP experience, solid understanding of GxP and clinical trial operations
Associate Director, Pharmacovigilance
PharmD or RN degree, experience in pharmacovigilance or clinical development, and proficiency in Microsoft Office Suite
Senior Director, Clinical Development
8+ years of experience in clinical research, MD with board certification, and experience in rare diseases or neurology
Senior Clinical Trial Associate
5+ years of experience, CTA experience, knowledge of global regulatory requirements, experience with clinical trial systems
Vice President, Corporate and Internal Communications
10+ years of communications experience, exceptional writing and storytelling skills, and ability to balance strategic thinking with hands-on execution
Senior Manager, Centralized Monitoring
5+ years of clinical research experience, CRA experience, and RN or equivalent clinical/medical background
Associate Director, Clinical Operations
10+ years of experience in the pharmaceutical or medical device industry, excellent knowledge of international regulatory and ICH GCP guidelines, and the ability to manage large complex budgets
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