Senior Site Management and Monitoring Oversight Lead

CSL's R&D organization is accelerating innovation to deliver greater impact for patients. With a project‑led structure and a focus on collaboration, we’re building a future‑ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide.

Your Opportunity

Reporting to the Senior Director Head of Site Management and Monitoring, you will be accountable for the strategic and operational oversight of investigational site management and monitoring activities across assigned clinical studies or programs. This role ensures that clinical trials are executed with high quality, regulatory compliance, and operational efficiency, in alignment with global clinical development strategies.

Operating within a matrix environment, you will partner with internal stakeholders and external service providers to develop and implement study‑specific oversight plans, monitor site performance, and proactively identify and mitigate risks. The role is pivotal in maintaining sponsor oversight, validating the effectiveness of site‑level activities, and ensuring that monitoring plans and tools adequately address protocol‑specific risks.

Your Responsibilities will include

• Site Oversight Execution : Ensure effective sponsor oversight of investigational sites by reviewing monitoring visit reports, site communications, and issue resolution documentation.
• Monitoring Plan Implementation : Support the development and execution of study‑specific monitoring plans, ensuring alignment with protocol requirements and risk‑based monitoring strategies.
• Performance Tracking : Monitor site‑level performance metrics (e.g., enrollment, data quality, protocol adherence) and elevate concerns to study leadership as needed.
• Vendor Collaboration : Partner with CROs and external service providers to ensure consistent and compliant site management practices across assigned studies.
• Compliance & Inspection Readiness : Contribute to audit and inspection preparedness by validating site documentation, ensuring timely issue resolution, and maintaining oversight logs.
• Primary point of contact for study‑related matters both internally and externally (e.g., vendors).
• Maintain up‑to‑date knowledge of the therapeutic area / product candidate(s), clinical practice, competitors, and regulatory considerations.
• Support audits / inspections and resolution of findings.
• Assist in the development of new SOPs, guidelines, etc., and participate in working groups on new processes.

Your Skills & Experience

Our Benefits

We encourage you to make your well‑being a priority. It’s important and so are you. Learn more about how we care at CSL.

About CSL

CSL is a leading global biotechnology company with a dynamic portfolio of life‑saving medicines, including those that treat haemophilia and immune deficiencies, as well as vaccines to prevent influenza. Since our start in 1916, we have been driven by our promise to save lives through innovation.

We want CSL to reflect the world around us

At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future.

Do work that matters at CSL!

Join a team where your contributions make a real difference. Make work that matters at CSL.

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