Join the Oncology Voice Network. Join for Free
Back to Career Growth Hub

Join free to apply and get matched.

Browse roles anytime — create a free OVN account to apply and stay visible to employers.

Connect Life Sciences logo

Medical Monitor, Board Certified, Hematology/Oncology

Connect Life Sciences · Bridgewater, NJ

Visit company website
FULL-TIME Posted Oct 7, 2026

Job Description

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.

Additional Details

City
Bridgewater
State
New Jersey
Country
US
Apply Now

Apply and matching require a free OVN account. Browse listings anytime without signing in.

Browse all jobs · More roles at Connect Life Sciences