Medical Monitor/Senior Medical Monitor, Hematology

Role: Medical Monitor for Tessera's hematology-focused gene writing clinical programs, overseeing early-stage trials targeting diseases like sickle cell and hematologic malignancies. Responsibilities: provide medical oversight, review safety, eligibility, and data integrity; support protocol development and regulatory activities; engage with investigators, CROs, and cross-functional teams; contribute to safety assessments and clinical strategy. Requirements: MD or MD/PhD with board certification in Hematology or Hematology/Oncology, 3+ years in biotech/pharma clinical development, experience serving as Medical Monitor, strong understanding of hematologic disorders, regulatory knowledge, and safety monitoring skills. Preferred: experience with rare hematologic and genetic diseases, cell/gene therapies, early-phase trials, regulatory submissions, and DMC support. High-Value: hematology/oncology, gene therapies, early-phase (Phase 1/2), regulatory compliance, global safety monitoring, cross-disciplinary collaboration. WorkSetup: hybrid at Somerville, MA; 10–20% travel.