Senior Director Head of Site Management and Monitoring Oversight

New Yesterday

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.
The Head of Site Management and Monitoring is a senior leadership role accountable for the strategic direction, operational execution, and quality
oversight of global site monitoring activities across all phases of clinical development. This role is pivotal in ensuring that clinical trial execution meets
regulatory, ethical, and scientific standards while enabling operational excellence in a highly outsourced environment.
Roles & Responsibilities
Strategic Oversight and Quality Governance:
​ Provide executive leadership in the development, execution, and continuous optimization of global oversight frameworks, including Monitoring
Oversight Visits, Compliance Oversight Programs, and site-level risk mitigation strategies. Oversee GCP compliance and data integrity across a global
footprint of more than 1,300 clinical trial sites and over 31,000 participants, ensuring alignment with enterprise risk and quality objectives.
​
Operational Excellence in Monitoring:
​ Drive strategic oversight of site management and monitoring activities across all phases of clinical development. Ensure global execution is fully
aligned with protocol-specific risk assessments, regulatory requirements, and development timelines. Ensure the CRO(s) maintain high-quality,
inspection-ready operations while proactively identifying and resolving site-level issues in a dynamic environment.
​
CRO and FSP Governance:
​ Lead governance of and oversight of Clinical Research Organization (CRO) partnerships. Act as a key strategic partner and influencer with CRO
leadership, building strong relationships to drive accountability, resolve quality and performance issues—often
on a daily basis
given the operational
scale—and ensure delivery to protocol and regulatory expectations.
​
Cross-Functional Leadership and Regulatory Readiness:
​ Partner with Clinical Operations, Quality Assurance, Regulatory Affairs, and CRO stakeholders to ensure global site performance, inspection readiness,
and continuous improvement. Serve as the escalation lead for site-level quality and compliance issues, ensuring timely resolution, documentation,
and alignment with regulatory standards and internal SOPs.
​
Leadership and Capability Development:
​ Lead a geographically dispersed team, fostering a culture of agility, accountability, and performance. Develop internal talent and oversee CRO
capabilities to ensure consistent, high-quality oversight across a complex and evolving clinical operations landscape.
​
Innovation and Risk-Based Monitoring Enablement:
​ Champion the advancement of oversight technologies, dashboards, and analytics to support proactive, risk-based monitoring and data-driven
decision-making. Drive innovation to meet the demands of large-scale, global clinical operations and deliver continual process optimization
Qualifications & Experience Requirements Minimum undergraduate degree in life sciences or health/medical-related field; advanced degrees
preferred.
​
12+ years of experience in clinical operations, with a strong background in site monitoring and vendor
oversight.
​
Proven leadership in managing global teams and implementing oversight strategies for site
operations.
​
Deep understanding of ICH-GCP, regulatory frameworks, and best practices in sponsor
oversight.
​
Strong analytical, communication, and stakeholder engagement
skills
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 Behring
CSL Behring
is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives.
CSL Behring operates one of the world’s largest plasma collection networks,
CSL Plasma . Our parent company,
CSL , headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries. 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. Learn more
Inclusion and Belonging | CSL
Do work that matters at CSL Behring!
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Location:
Maidenhead
Job Type:
FullTime

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