Associate Director, Pharmacovigilance

About Us We are developing potentially best in class therapies for patients living with severe autoimmune diseases. Our lead antibody, claseprubart (DNTH103), is purposefully engineered with extended half-life, improved potency, and high selectivity for only the active C1s complement protein that drives disease pathology – enabling less frequent and more convenient self-administered subcutaneous injections. Our second clinical candidate, DNTH212 is a first and potentially best in class, bifunctional inhibitor that targets clinically validated and complementary disease modifying mechanisms, Type 1 IFN suppression and B cell modulation – enabling potential for improved clinical outcomes and patient friendly convenient, self-administered subcutaneous injections. To learn more, please visit www.dianthustx.com and follow us on LinkedIn . About the Role As the Associate Director, Pharmacovigilance, you will work closely with the Safety team to support ongoing clinical trials. This role is critical in ensuring patient safety and regulatory compliance throughout the drug development lifecycle. Day to day, you will work closely with safety physicians, clinical teams, and external stakeholders to manage safety data and contribute to safety oversight. You must have experience reviewing adverse events, safety signals, and coordinate/contribute to the Safety Review Committee (SRC) and Drug Safety Monitoring Boards (DSMB) meetings. You must have experience supporting clinical pharmacovigilance activities and working with DSMBs in order to be successful in this role. This is a unique role that will allow you to work collaboratively with the growing pharmacovigilance team that is working closely with cross functional teams to help Dianthus elevate the care of our patients' lives. We are building a culture of individuals who hold our core principles at the center of our operations, with the goal to elevate the care of our patients' lives. We are open to you working remotely within the United States. Key Responsibilities Safety Data Review Oversee pharmacovigilance activities for assigned clinical programs, ensuring alignment with global regulatory requirements and internal SOPs. Review, evaluate, and provide managerial oversight of adverse event (AE) reports, including serious adverse events (SAEs), ensuring accurate assessment and timely submission to regulatory authorities and ethics committees. Ensure quality and accuracy of safety data review within the safety database and direct reconciliation efforts with clinical databases to maintain data integrity. Cross-functional Communication & Collaboration Contribute to the development of safety sections within clinical documents, including protocols, investigator brochures, and clinical study reports. Manage and oversee the scheduling, planning, and facilitation of DSMB and SRC meetings, including preparation of agendas, meeting materials, guided discussions, documentation of minutes, and follow-up on action items. Contribute strategically to the preparation of aggregate safety reports such as the DSUR. Partner with safety physicians on signal detection, emerging safety issues, risk assessments, and benefit–risk evaluations. Serve as a subject matter expert to internal stakeholders and external partners on safety-related topics, providing guidance and ensuring consistent communication. Documentation & Compliance Ensure organizational compliance with global pharmacovigilance regulations (FDA, EMA, ICH) and company policies. Manage and oversee pharmacovigilance-related quality events, including change controls, deviations, and CAPAs, ensuring timely resolution and documentation. Supervise and ensure accurate documentation of DSMB and SRC meetings and maintain records within designated systems and repositories. Experience Education: PharmD or RN degree required. Experience in pharmacovigilance or in clinical development within biotech or pharmaceutical industry. Proven experience reviewing adverse events and working closely with safety physicians. Hands-on experience supporting DSMBs and SRCs and preparing safety deliverables. Proficiency in Microsoft Office Suite and Microsoft Teams, with the ability to leverage these tools for efficient communication, scheduling, and documentation Strong knowledge of global PV regulations (FDA, EMA, ICH guidelines). Excellent analytical, organizational, and communication skills. Ability to thrive in a fast-paced, start-up environment and manage multiple priorities. Fluency with Argus safety database Familiarity with rare disease or oncology programs. Prior experience in a start-up or small biotech setting.