Senior Director, Global Site Contracts

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.

General Description:

The Senior Director, Global Site Contracts is a strategic leadership position responsible for the global oversight, execution, and continuous improvement of clinical site contracting activities supporting sponsored clinical trials worldwide. This role provides leadership for site contract strategy, governance, operational delivery, and process optimization across all regions to ensure rapid study startup, compliant contract execution, and high-quality operational performance.

The position partners closely with Clinical Operations, Legal, Finance, Global R&D Sourcing, Compliance, CROs, and external institutions to establish and maintain scalable contracting processes, global standards, negotiation strategies, and performance metrics. The role is expected to drive operational excellence through innovative solutions, standardized methodologies, data-driven decision-making, and strong stakeholder alignment.

As a member of the Clinical Business Operations leadership team, this individual contributes to organizational strategy, workforce planning, vendor management, and functional transformation initiatives that support the evolving needs of the clinical development portfolio.

Key responsibilities include:

Lead and manage the Global Contracts Management team

Oversee activities related to the execution of clinical site contract documents and associated processes.

Develop and enhance policies, procedures, and systems that optimize contracting operations

Ensure compliance, quality, and efficiency across global contracting activities

Provide training, mentorship, and supervision to the contracts team

Essential Functions of the Job:

Strategic Leadership & Functional Governance

• •Develop and execute the global strategy, vision, governance framework, and operating model for Clinical Site Contracts, ensuring alignment with Global Clinical Operations (GCO) objectives and portfolio priorities
• •Serve as a member of the Clinical Business Operations Leadership Team, contributing to functional strategy, organizational planning, risk management, and operational excellence initiatives
• •Develop and oversee global governance models, portfolio plans, project plans, and operational frameworks that support efficient and compliant clinical site contracting activities
• •Determine, implement, and continuously evolve global policies, procedures, SOPs, templates, playbooks, and best practices for site contract management
• •Identify and maintain a globally consistent contract negotiation model that balances speed, compliance, quality, and business needs across regions

Global Site Contract Lifecycle Management

• •Provide global oversight and accountability for the management of all clinical contract agreements, including but not limited to:
• •Clinical Trial Agreements (CTAs)
• •Investigator Agreements
• •Confidential Disclosure Agreements (CDAs)
• •Site Master Service Agreements (MSAs)
• •Pharmacy Agreements
• •Ancillary Agreements
• •Consulting Agreements
• •Subcontractor Agreements
• •Other agreements supporting the clinical trial lifecycle.

• •Ensure timely development, negotiation, execution, amendment, maintenance, and close-out of global site contracts in support of study startup and study conduct milestones
• •Serve as the senior escalation point for complex contractual negotiations, site-specific issues, and institutional contracting challenges
• •Directly participate in high-priority or complex site negotiations when required
• •Maintain oversight of contract quality, compliance, and execution consistency across all regions and programs

Study Startup Strategy & Risk Management

• •Partner with Clinical Operations, CROs, and study teams to identify country-, site, and study-specific contracting risks that could impact startup timelines, enrollment, or study execution
• •Develop and implement proactive risk mitigation strategies to accelerate study startup and reduce contracting delays
• •Conduct regular risk reviews against study and portfolio milestones, identifying and escalating potential risks to timelines and deliverables
• •Leverage contracting intelligence, market insights, and operational metrics to support study feasibility, planning, and startup execution
• •Provide strategic oversight and guidance on study startup activities and contracting dependencies across the portfolio

Cross-Functional Collaboration

• •Collaborate closely with Clinical Operations, Legal, Compliance, Finance, Tax, Procurement, Clinical Outsourcing, and Development stakeholders to ensure successful execution of clinical trial contracting strategies
• •Partner with Contract Managers, Legal Counsel, Contract Associates, and Site Contract leaders throughout the contract lifecycle to resolve issues and drive timely agreement execution
• •Maintain effective relationships with investigator sites, institutions, CROs, vendors, and strategic partners
• •Communicate contract status, negotiation progress, key risks, and critical path issues to senior leadership and study stakeholders on a regular basis
• •Serve as the primary escalation and decision-making point for complex contract and site budget issues

Site Budget & Financial Oversight

• •Partner with Site Payments, Finance, and Clinical Operations leaders to ensure alignment between negotiated budgets, payment terms, and contractual obligations.
• •Lead project review and governance meetings focused on contract performance, financial outcomes, startup effectiveness, and portfolio success
• •Review, analyze, and interpret contract negotiation reports, financial metrics, and operational performance indicators
• •Ensure budget and contract strategies support both business objectives and site relationship needs

Vendor & Client Relationship Management

• •Oversee governance and performance of contract service providers, FSP partners, CROs, and external vendors supporting clinical site contracting activities.
• •Establish and monitor KPIs, SLAs, quality standards, and productivity measures for internal teams and external partners
• •Maintain and strengthen strategic relationships with key internal stakeholders, investigator sites, institutions, and vendors
• •Support enterprise and portfolio-level stakeholder engagement through transparent communication, issue resolution, and operational leadership.
• •Drive solution-oriented approaches to address study, site, vendor, and departmental challenges

Essential Functions of the Job:

Strategic Leadership & Functional Governance

• •Develop and execute the global strategy, vision, governance framework, and operating model for Clinical Site Contracts, ensuring alignment with Global Clinical Operations (GCO) objectives and portfolio priorities
• •Serve as a member of the Clinical Business Operations Leadership Team, contributing to functional strategy, organizational planning, risk management, and operational excellence initiatives
• •Develop and oversee global governance models, portfolio plans, project plans, and operational frameworks that support efficient and compliant clinical site contracting activities
• •Determine, implement, and continuously evolve global policies, procedures, SOPs, templates, playbooks, and best practices for site contract management
• •Identify and maintain a globally consistent contract negotiation model that balances speed, compliance, quality, and business needs across regions

Global Site Contract Lifecycle Management

• •Provide global oversight and accountability for the management of all clinical contract agreements, including but not limited to:
• •Clinical Trial Agreements (CTAs)
• •Investigator Agreements
• •Confidential Disclosure Agreements (CDAs)
• •Site Mast