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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.

About Us BeOne is a global oncology company that is discovering and developing creative treatments that are more affordable and accessible to cancer patients worldwide. With a broad portfolio, we are expediting development of our diverse pipeline of novel therapeutics through our internal capabilities and collaborations. We are committed to radically improving access to medicines for far more patients who need them. Our growing global team of more than 10,000 colleagues spans five continents, with administrative offices in Basel, Beijing, and Cambridge, U.S. To learn more about BeOne, please visit www.beonemedicines.com and follow us on LinkedIn and X (formerly known as Twitter).

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.

Job Description General Description: The Contract Lifecycle Manager is responsible for oversight and on time execution of all regional clinical contract agreements including, but not limited to, Clinical Trial Agreements (CTAs), investigator agreements, confidentiality agreements, ancillary agreements, pharmacy agreements, site master service agreements, consulting agreements, single-service,



subcontractor agreements among other agreements in the clinical contract space.

Essential Functions Of The Job

Functional line management of the regional based Clinical Contracts team including Contract Managers and Contract Associates or equivalent and delivers individual and group feedback to support ongoing development.

The Regional Site Contracts Lead may have authority through a POA to sign Investigator Contracts as authorized by BeOne Medicines Legal and Tax

Responsible for ensuring that the negotiation process is maintained and improved to meet the financial and operational needs of the BeOne Medicines.

Responsible for ensuring the negotiation of Clinical Site budgets is within Fair Market value and internal approval guidelines.

Partner with Clinical Operations teams, and CBO colleagues to improve overall Clinical Site Contract and budget metrics and implement processes.

Ensure standards are applied to the Clinical Site Contract and budget processes across project portfolios and support continuous improvement activities while developing TA-aligned strategies.

Serve as a regional escalation point for Clinical Site Contracts and provide regional oversight at the Program level.





Leverage leading industry tools and data sources to provide budget and contract feedback aligned with BeOne Medicines parameters and fair market value guidance.

Recognize and improve potential delays providing solutions to resolve and elevate nonperformance.

Provide oversight and guidance for clinical site contract negotiations, identify any potential risks, and be accountable for the overall contracting timelines/lifecycle in various regions.

Perform Regional level oversight of Clinical Site Contracts to ensure contracts in the region are completed per company standards/timelines. Implement mitigation plans as necessary in the assigned region.

Development and implementation of new policies and procedures based on identified needs

Other tasks and responsibilities as requested by departmental and company leadership.

Supervisory Responsibilities

Yes

Computer Skills

Microsoft Office apps, CTMS, Contract Lifecycle Management System, Veeva, Jira, Sharepoint etc.

Qualification Required Education Required:

Bachelor’s degree; JD highly preferred or 8+ years of outstanding experience managing and negotiating clinical trial agreements and budgets

Experience in the CRO or pharmaceutical industry is essential.

Other Qualifications

Good knowledge of ICH-GCP, pharmaceutical related regulations and laws;

Good understanding of clinical trial contracting process, and relevant clinical operation practices;

Awareness and understanding of compliance and regulatory matters in clinical research

Proven negotiation, interpersonal and business skills

Strong planning and organizational skills and the ability to work independently and effectively in a dynamic environment with competing priorities

Sense of urgency and strong goal orientat

📌 Regional Contracts Lead, Clinical Site Contracts (Sydney)
🏢 BeOne Medicines
📍 Sydney