• designs and implements initiatives that optimize clinical operations and enhance care delivery across aligned area(s), or the organization • provides strategic advice and guidance to functional team(s) • report to the Clinical Operations Strategy Principal • responsible for advancing and executing high-impact strategic initiatives across CenterWell's Value-Based Care Enablement / IPA business • serve as a trusted advisor to senior leadership • lead the development of forward-looking business models and go-to-market strategies • ensure the organization is positioned to scale innovative offerings and remain competitive in a rapidly evolving healthcare landscape • drive the development of segment-level strategies and ensure successful execution across complex, cross-functional environments • operate as an advanced subject matter expert across clinical quality, business operations, and technology to support value-based care enablement • lead highly complex initiatives from concept through scaled execution, applying deep business acumen, structured problem-solving, and innovative solution design to drive measurable improvements in financial performance, operational efficiency, and membership growth

• Oversight of planning, drafting, negotiating, tracking, and execution of site/investigator contracts which may be subcontracted to an external service provider or managed internally • Ensures final contracts are delivered to agreed timelines, within Fair Market Value & in compliance with relevant legal and regulatory requirements. • Provide study-level oversight and guidance for clinical site contract negotiations, identify any potential risks, and be accountable for the overall contracting timelines/lifecycle in various regions. • Serve as the study-specific point of contact with the BeiGene Clinical Operations team and legal team on-site/investigator contract and budget matters. • Oversee a team of Site Contract Associates or equivalent at a Project level to ensure contracts in the region are completed per company standards/timelines. • Implement mitigation plans as necessary in the assigned region. • Serve as an escalation point for unresponsive sites, site budget negotiations and ensure costs are approved within BeiGene FMV standards. • Adapts CBO’s plan and priorities to address resource and operational challenges • Training and mentoring of new members of the local Contracts Team regarding financial/contractual issues and sharing experiences. • Contribute to process improvements, knowledge transfer and best practice sharing. • Ensure all agreements are executed in a timely manner, contributing to efficient site start-up timelines. • Organizes and prioritizes multiple initiatives and sets clear plans for delivery • Effectively escalate/communicate to stakeholders and clinical teams in a professional and timely manner regarding contract issues that could impact project deliverables. • Responsible for management and administration of contracts and ensures compliance with corporate policies. • Serve as a backup to Site Contract Associates, as needed to handle out-of-office coverage. • Ensure proper delivery of fully executed clinical site contracts to CBO Payments teams and liaison with CBO payments team, as necessary. • Provide substantive guidance, monitoring, and support regarding clinical site contract deliverables, including undertaking activities identified in the CBO Roles/Responsibilities and/or Study Management Plan. • Review, apply, and maintain BeiGene Playbook to enhance the efficiency of negotiation in conjunction with BeiGene Legal. • Responsible for overseeing a Clinical Research Organization responsible for contract negotiations (if applicable). • Responsible for clinical contract management, study metric tracking and reporting. • Active participant in various study meetings. • Prepare program/study status reports. • Maintains a system for tracking progress and status of clinical budget/contracts. • Support activities of various contracts and subsequent contract amendments note to files and other contract-related requests. • Assist colleagues with the resolution of problems related to site budget, contract terms and conditions, compliance with BeiGene policy, and any other site contract-related issues. • Deliver training to CBO colleagues or other Business Units as needed. • Serve as a point of escalation for sites that are unresponsive or slow to negotiate. • Create and develop effective contract templates and tools • Performs other duties as assigned by management.

• Accountable for project delivery with regards to agreed time, scope, cost, and quality. • Serve as key client contact for assigned projects, establishing working relationships with client project teams. • Lead core project teams and facilitate effective cross-functional teamwork among project members. • Proactively identify and resolve conflicts as needed. • Understand the project delivery strategy, costing assumptions and resulting budget for assigned projects. • Deliver projects to scope, schedule, and costs, ensuring all remain on track with the contract and financial performance targets. • Proactively lead both quality control and risk assurance activities to ensure project deliverables are met. • Ensure that all staff allocated to assigned projects adheres to professional standards and SOPs. • In collaboration with relevant departments, prepare and deliver presentations for new business as required.

• Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP and/or Good Pharmacoepidemiological Practices (GPP) and protocol compliance • Uses judgment and experience to evaluate overall performance of site and site staff and to provide recommendations regarding site-specific actions • Maintains a working knowledge of ICH/GCP Guidelines or other applicable guidance, relevant regulations, and company SOPs/processes • Verifies the process of obtaining informed consent has been adequately performed and documented for each subject/patient • Assesses factors that might affect subject/patient’s safety and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues