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Medical Monitor, Board Certified, Hematology​/Oncology

Job in Bridgewater, Plymouth County, Massachusetts, 02324, USA
Listing for: International Society on Thrombosis and Hemostasis
Full Time position
Listed on 2026-10-10
Job specializations:
  • Doctor/Physician
Salary/Wage Range or Industry Benchmark: 180000 - 240000 USD Yearly USD 180000.00 240000.00 YEAR
Job Description & How to Apply Below
Medical Monitoring & Patient Safety Oversight — Lead Program
  • Serve as the medical monitor for the program’s studies, providing real-time clinical judgment on eligibility, dose modifications, premedication compliance, and management of class-specific toxicities (e.g., effusions/edema, cutaneous reactions, hepatic abnormalities, hematologic toxicity).
  • Perform detailed clinical data review of patient data profiles and other eCRF data (including drafting data queries, discussion of patient cases with Investigators, etc.).
  • Lead ongoing benefit-risk assessment, including review of SAEs, AESIs (PBD-ADC class effects), and emerging safety signals; partner with Pharmacovigilance, DSMC/iDMC, and Biostatistics to ensure timely signal detection and risk mitigation.
Cross-Functional Partner
  • Partner with Translational Medicine, Biomarkers, and Biostatistics to characterize patient outcomes on the study drug (including by COO/GCB vs. non-GCB, double/triple-hit status, prior CAR-T exposure, and age/frailty), informing label strategy and lifecycle planning.
Quality, Compliance & Inspection Readiness
  • Ensure all medical monitoring and sBLA activities are conducted in compliance with ICH-GCP, FDA/EMA regulations, and internal SOPs; maintain audit- and inspection-ready documentation of clinical decisions and benefit-risk rationale in preparation for pre-approval inspections (BIMO) and sponsor inspections.
Qualifications
  • MD required; MD/PhD preferred.
  • Board certification in Hematology/Oncology (in U.S. clinic preferred).
  • Some clinical experience treating aggressive B-cell lymphomas (DLBCL, HGBCL, transformed FL) strongly preferred.
  • 15+ years of clinical R&D experience in biopharma (or a combination of clinical and industry experience).
  • Direct experience with antibody-drug conjugates (ADCs) — particularly PBD-based or CD19-targeted agents.
  • Familiarity with the evolving DLBCL treatment landscape and ability to position the asset strategically within it.
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