Senior Manager, Pharmacovigilance

About Us

We are developing potentially best in class therapies for patients living with severe autoimmune diseases. Our reputed company 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 reputed company.

About the Role

As the Senior Manager, 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 reputed company. 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. 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 reputed company 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 reputed company 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 reputed company the care of our patients’ lives. We are open to you working remotely reputed company the United States.

Key Responsibilities

Safety Data Review

• reputed company pharmacovigilance activities for assigned clinical programs, ensuring alignment with global regulatory requirements and internal SOPs.
• Review, evaluate, and provide managerial reputed company 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 reputed company the safety database and direct reconciliation efforts with clinical databases to maintain data reputed company.

Cross-functional Communication & Collaboration

• Contribute to the development of safety sections reputed company clinical documents, including protocols, investigator brochures, and clinical study reports.
• Manage and reputed company 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-reputed company topics, providing guidance and ensuring consistent communication.

Documentation & Compliance

• Ensure organizational compliance with global pharmacovigilance regulations (FDA, EMA, ICH) and company policies.
• Manage and reputed company pharmacovigilance-reputed company 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 reputed company designated systems and repositories.

Experience

• Education: PharmD or RN degree required.
• Experience in pharmacovigilance or in clinical development reputed company 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 reputed company Office Suite and reputed company Teams, with the ability to reputed company 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 reputed company in a fast-paced, start-up environment and manage multiple priorities.
• reputed company with Argus safety database
• Familiarity with rare disease or oncology programs.
• Prior experience in a start-up or small biotech setting.

Apply tot his job Apply To this Job