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Legend Biotech USA, Inc.

Advanced degree preferred.7+ years of pharmaceutical, biotech, CRO, or related clinical research experience; 10+ years preferred.Experience working with data sources to inform trial forecast ...

Legend Biotech USA, Inc.

$127K - $167K/yr

Advanced degree preferred.7+ years of pharmaceutical, biotech, CRO, or related clinical research experience.Strong experience in vendor oversight, outsourcing, site contracts, investigator payments ...

Legend Biotech USA, Inc.

Advanced degree preferred.7+ years of pharmaceutical, biotech, CRO, or related clinical research experience.Experience in clinical operations with exposure to sample management, lab operations, or ...

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Infographic showing various Biotech Cro job openings in the United States as of May 2026, with employment types broken down into 100% Full Time. Highlights an 33% Hybrid, and 67% Remote job distribution, with an average salary of $113,048 per year, or $54.4 per hour.

Manager, Site Contracts & Payments Management

Legend Biotech US

Somerset, NJ • Hybrid

$94K - $125K/yr

Other

Posted 27 days ago

Job description

Legend Biotech is seeking a Manager, Site Contracts & Payments Management as part of the Clinical Operations team based in Somerset, NJ.

Role Overview

The Site Contracts & Payments Manager is responsible for site contracting and investigator payment process oversight and management, and vendor due diligence across Legend pipeline studies. The role serves as a central point of accountability for improving operational effectiveness, financial discipline, and sponsor-CRO-site workflow alignment for site contracting and payment processes.

Key Responsibilities

  • Partner with CROs to develop and oversee process workflows, and create visibility into site contract and investigator payment workflow efficiency across studies.
  • Partner with CROs, AP, Procurement, Finance, Legal, and study teams to align process workflows, identify gaps, and improve efficiency in contracting and payment execution.
  • Monitor key milestones, bottlenecks, and escalations affecting site startup experience for contracting, payment timeliness, and financial predictability.
  • Support reconciliation, issue resolution, and continuous improvement related to site contracting and investigator payment operations.
  • Coordinate vendor due diligence and risk assessment activities with Procurement, Finance, QA, and other stakeholders.
  • Performs other duties as required.

Requirements

  • Minimum degree requirements of a bachelor's degree (BA, BS) in scientific, health care, business, or related discipline. Advanced degree preferred.
  • 7+ years of pharmaceutical, biotech, CRO, or related clinical research experience.
  • Strong experience in vendor oversight, outsourcing, site contracts, investigator payments, or related operational functions required.
  • Experience working cross-functionally with AP, Procurement, Finance, and Legal required.
  • Experience working in SAP/4 Hanna preferred.
  • Experience establishing KPIs and oversight models preferred.
  • Oncology, cell therapy, or early-phase clinical operations experience preferred.
  • Ability to travel as necessary (up to 10%).
  • Effective oral, written, and interpersonal communication skills.
  • Strong process management, organizational, and problem-solving skills.
  • Ability to identify operational risk and drive practical mitigation strategies.
  • Strong project management skills and the ability to manage multiple priorities.
  • Computer literacy required (MS Word, MS Excel, MS PowerPoint, MS Project).
  • Working knowledge of GCP, FDA, and ICH Guidelines.

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