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The Principal Scientist/ Associate Director will be a key member of Acrivon Therapeutics Clinical Development team and lead our clinical science efforts to support the development of two clinical stage assets currently being evaluated in cancer patients (ACR-368 and ACR-2316). This role will drive real-time analysis and monitoring of emerging clinical data (both safety and clinical activity) and will be a key contributor in all future clinical studies executed by Acrivon in terms of design, data collection, and data interpretation.