Seeking a Director of Pharmacovigilance and Safety Science to lead safety surveillance, adverse event reporting, and risk management for clinical programs in nephrology and cardiometabolic diseases. Responsibilities include overseeing safety management plans, case processing, aggregate safety reports, and regulatory submissions, as well as managing CRO/vendor partnerships. The role involves collaborating with cross-functional teams, presenting data to stakeholders, and supporting safety governance. Candidates should have an advanced degree in health sciences with 4+ years of experience in drug safety, knowledge of PV regulations, medical review, and risk mitigation. Strong leadership, adaptability, and the ability to travel domestically are essential.