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Job Overview
Location
2 Locations
Job Type
Full-time
Category
Operations
Date Posted
April 8, 2026
Full Job Description
đź“‹ Description
- • The Director, Regional Head Site Management & Oversight provides strategic leadership for clinical site operations across the EMEA region, ensuring effective conduct and supervision of site management activities and oversight for clinical programs in alignment with CSL’s overall strategy, regulatory standards, and delivery timelines and budgets.
- • Day to day, the role involves operational oversight of site health and monitoring activities, supporting QA audit and inspection planning, implementing CAPAs, identifying and mitigating site-level risks impacting recruitment, retention, data quality, or compliance, providing study support on escalated site issues, supporting sites in understanding study expectations and timelines, ensuring effective site recruitment planning and delivery, responding to recruitment issues from investigators/CROs, building and maintaining strong relationships with investigators and site staff, serving as the sponsor’s primary point of contact for assigned studies, understanding site capabilities and constraints to improve engagement, collecting site feedback to advocate for process simplification, identifying opportunities to improve study materials and operational processes, representing the “voice of the site” in cross-functional discussions, providing local site intelligence to feasibility teams, and supporting site development. This role requires travel to investigator meetings, sites, and CROs, with anticipated travel exceeding 50%.
- • CSL Limited is a global biotherapeutics leader headquartered in Melbourne, Australia, employing 32,000 people and delivering lifesaving therapies to over 100 countries. CSL Behring, a division of CSL, focuses on innovative therapies in immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas using plasma fractionation, recombinant protein technology, and cell and gene therapy platforms. The company operates one of the world’s largest plasma collection networks, CSL Plasma, and is committed to inclusion, belonging, and equal opportunity employment.
- • In this role, the individual can develop strategic leadership in global clinical site management, deepen expertise in regulatory compliance (ICH/GCP), enhance vendor and CRO oversight capabilities, strengthen stakeholder engagement with HCPs and Medical Affairs, drive process improvements in clinical trial execution, and grow mentorship and coaching skills while contributing to the delivery of innovative therapies that address unmet medical needs and improve patient lives.
🎯 Requirements
- • Bachelor’s degree or equivalent in life science, nursing, pharmacy, or medical laboratory technology
- • 12+ years of relevant clinical research experience within the pharmaceutical industry
- • Proven experience leading and managing professional teams in site management, monitoring, and overseeing large and/or complex global clinical trials
- • Thorough knowledge of ICH guidelines/GCP and its applicability across all stages of clinical development
- • Demonstrated experience overseeing vendors and CROs
- • Excellent understanding of all tasks in a clinical development program from protocol development to finalizing a clinical study report
🏖️ Benefits
- • Opportunity to work with a global biotherapeutics leader committed to saving lives through innovative therapies
- • Commitment to inclusion, belonging, and a culture of curiosity and empathy that fosters innovation and strong stakeholder relationships
- • Equal Opportunity Employer with support for reasonable accommodations during the application process
- • Access to CSL’s well-being resources and benefits programs (details available via CSL careers portal)
- • Platform to drive meaningful impact in clinical trial execution and patient outcomes across immunology, hematology, cardiovascular, metabolic, respiratory, and transplant therapeutic areas
Skills & Technologies
GCP
Onsite
About CSL Limited
Global biotechnology company headquartered in Melbourne, Australia. Develops, manufactures and markets biotherapies to treat rare and serious diseases, including plasma-derived therapies, recombinant proteins and vaccines through CSL Behring and Seqirus divisions. Serves patients in more than 100 countries with R&D, manufacturing and commercial operations across North America, Europe, Asia and Australia.
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