Medical Monitor/Senior Medical Monitor, Hematology

Provide medical oversight for early clinical studies of Tessera’s Gene Writing therapies for hematologic disease. Work includes reviewing eligibility, safety findings and clinical laboratory data, advising investigators, contributing to study designs and interpreting efficacy and biomarker results. The role supports development in indications such as sickle cell disease and hematologic malignancies. Based in Somerville, Massachusetts, with hybrid working and approximately 10–20% travel.

MD, MD-PhD or equivalent with hematology, hematology/oncology or appropriately related specialist expertise. Requires at least three years of industry clinical development with medical-monitor experience, or extensive academic experience leading hematology/oncology trials. Early-phase and cell/gene therapy experience are preferred.