CSL Seqirus is hiring a Lead Clinical Site Ambassador to be accountable for the strategic and operational oversight of investigational site management and monitoring activities. This role ensures clinical trials are executed with high quality, regulatory compliance, and operational efficiency, in alignment with global clinical development strategies.
What You’ll Do
- Provide operational oversight of the site, site health, and monitoring activities.
- Identify and proactively mitigate site-level risks impacting recruitment, retention, data quality, or compliance, in partnership with CROs.
- Support QA audit and inspection planning, and implementation of CAPAs as needed.
- Provide study support on escalated site issues related to study delivery by coordinating communications and resolution efforts.
- Support sites in understanding study expectations, timelines, and required deliverables.
- Be accountable for effective site recruitment planning and delivery, consistent with global and/or country plan and local targets in collaboration with CROs.
- Responsible for enrollment support and ensure progress by responding to recruitment issues from investigators and CROs.
- Build and maintain strong, trusted relationships with investigators and site staff as the face of CSL.
- Serve as the sponsor primary point of contact for assigned studies.
- Understand site capabilities, constraints, and strategic priorities to improve site engagement and long-term collaboration.
- Collect feedback from sites and advocate for process simplification and burden reduction internally.
- Identify opportunities to improve study materials and operational processes.
- Represent the “voice of the site” in cross-functional discussions and initiatives.
- Provide local site intelligence to feasibility teams.
- Support site development.
What We’re Looking For
- Bachelor’s degree or equivalent in life science, nursing, pharmacy, or medical laboratory technology.
- 10+ years clinical research experience within the pharmaceutical industry.
- Experience in leading or managing a team as well as in site management, monitoring and overseeing large and/or complex global clinical trials.
- Strong understanding and experience in the drug development process and specifically each step within the clinical trial process.
- Strong budget forecasting and management experience.
- Extensive experience and knowledge of ICH guidelines/GCP and its applicability to all stages of the clinical development process.
- Excellent understanding of all tasks involved in a clinical development program(s) from developing a protocol through to finalizing a clinical study report.
Team & Environment
You will operate in a matrix environment, partnering with internal stakeholders and external service providers.
Work Mode
This is a remote position.
CSL is an Equal Opportunity Employer. Inclusion and belonging is at the core of our mission and fuels our innovation. 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.
