Associate Medical Director, Pharmacovigilance

<div class="content-intro"><p><strong><u>Company Overview</u></strong></p> <div class="x_elementToProof" data-olk-copy-source="MessageBody"> <div data-olk-copy-source="MessageBody">Immunome is a clinical-stage targeted oncology company committed to developing first-in-class and best-in-class targeted cancer therapies. We are advancing an innovative portfolio of therapeutics, supported by a leadership team with deep experience in the design, development, and commercialization of cutting-edge therapies, including antibody-drug conjugates. Our pipeline includes varegacestat, an investigational gamma secretase inhibitor for which an NDA has been accepted by the U.S. FDA; IM-1021, a clinical-stage ROR1 ADC; IM-1617, a clinical-stage solid tumor ADC; and IM-3050, a clinical-stage FAP-targeted radioligand therapy. We are also advancing a broad portfolio of early-stage ADCs pursuing undisclosed solid tumor targets.</div> </div></div><p><strong><u>Position Overview</u></strong></p> <p>The Associate Medical Director, Pharmacovigilance (PV) will provide medical leadership and oversight of safety management activities across Immunome’s early phase oncology portfolio. This position will provide safety oversight for the detection, evaluation, interpretation, and communication of safety information across assigned oncology assets. Within the Pharmacovigilance function, they will be responsible for driving proactive safety surveillance, risk management, and signal detection throughout the product lifecycle - from early clinical development through post-marketing.&nbsp;</p> <p>The ideal candidate will be a medically trained professional with an understanding of global pharmacovigilance regulations, and experience in a biotech or pharmaceutical setting. The individual should be comfortable working in a fast-paced, science-driven organization with investigational therapies, evolving safety profiles, and complex patient populations across internal departmental functions.&nbsp;</p> <p><strong><u>Responsibilities</u></strong></p> <p><strong>Leadership in Drug Safety</strong>&nbsp;</p> <ul> <li>Provide&nbsp;medical&nbsp;oversight and leadership for all safety activities related to assigned products, ensuring patient safety across development and post-marketing phases.&nbsp;</li> <li>Provide medical review, interpretation, and assessment of adverse events, serious adverse events, suspected adverse reactions, adverse events of special interest, deaths,&nbsp;discontinuations&nbsp;due to adverse events, and other clinically relevant safety data.&nbsp;</li> <li>Support&nbsp;safety management teams to develop, implement, and refine pharmacovigilance strategies in alignment