Senior TMF Lead (Senior Manager)

Work Environment:

• This is a hybrid position based in King of Prussia, PA or Maidenhead, UK with a minimum of 3 days onsite in the designated work location weekly.

Relocation and mobility assistance are not provided.

Position Overview:

Every clinical trial CSL runs depends on a documented, defensible record of how it was conducted — the Trial Master File. It's the evidence base regulators, auditors, and inspectors turn to when they need to know that a study was run to standard, from first patient in to final archive. Get the TMF right, and inspections go smoothly, submissions move forward, and study teams can focus on the science instead of scrambling for documentation. Get it wrong, and everything downstream slows down. We're looking for a Senior TMF Lead to take day-to-day ownership of that record across our full therapeutic portfolio — not as an administrative function, but as a genuine operational discipline with its own standards, technology, and continuous improvement agenda. You'll work closely alongside the Associate Director as a trusted partner on project management and TMF Operations standards, including people management, processes, and systems.

Key Responsibilities:

You'll provide oversight and hands-on management for a team supporting TMF operations across all of CSL's therapeutic areas, reporting to the Associate Director, TMF Operations — Portfolio Development Excellence, Process and Compliance. In practice, that means: TMF Governance & Process Management

• Develop and implement TMF oversight processes, support study teams with TMF tools, and drive updates to TMF-related processes and standards. TMF Systems & Innovation
• Oversee TMF technologies, eTMF enhancements, reference model updates, templates, tools, training, and continuous improvement initiatives aligned with industry best practices. Vendor & ESP Oversight
• Manage External Service Provider (ESP) performance to ensure TMF deliverables are achieved within quality, cost, and timeline expectations. Inspection & Audit Readiness
• Support internal and external inspections and audits by providing TMF expertise, facilitating document retrieval, and addressing findings. Metrics & KPI Management
• Establish, monitor, and report TMF metrics and KPIs to demonstrate inspection readiness and TMF completeness across the portfolio. Stakeholder Partnership
• Build and maintain strong relationships with global stakeholders, fostering collaboration, communication, accountability, and customer focus. Issue Resolution & Continuous Improvement
• Support study teams with TMF process and system escalations while driving efficiencies, quality improvements, and cost reduction initiatives. TMF Archiving Oversight
• Ensure compliant archiving of paper and electronic TMFs, including vendor coordination and adherence to TMF plans, SOPs, and retention requirements. eTMF Governance & Transfers
• Support eTMF business ownership, system requirements, process capabilities, and TMF transfer activities as needed. People Leadership & Team Development
• Lead, coach, mentor, and develop TMF staff; support recruitment, resource planning, performance management, and succession development.

Who you'll work with: You'll sit as a key stakeholder in the TMF Operations management team, working very closely with the Associate Director and Managers. In parallel, you'll work regularly with the Study File Specialists working across studies. Cross-functionally, TMF reaches all functions, and you'll build close relationships with Clinical Compliance, Study Management, and leaders across the organization. In addition, you'll collaborate with counterparts at various vendors and External Service Providers. It's a role built on relationships as much as process, and one where the quality of your judgment shows up in how ready CSL is, at any given moment, to open its files to an inspector and stand behind what's inside.

Minimum Qualifications:

6+ years of relevant clinical research experience in the pharmaceutical industry building, setting up, and maintaining Trial Master File infrastructure Bachelors Degree in life sciences, pharmacy, or another health/medical field; equivalent clinical research experience and relevant certifications (for example, an RN diploma/associates degree or certified medical technologist credential) will also be considered Demonstrated working knowledge of the regulatory landscape for global submissions, including

ICH GCP, FDA GCP

regulations, and EU Clinical Trials Regulations A track record of managing vendor oversight and of working in a formal management capacity Comfort operating across cross-functional, multicultural, international teams, and the judgment to make sound calls on complex, sometimes ambiguous, regulatory and operational questions Proven effective written and verbalcommunication skills, with the interpersonal range to work independently and as part of a team Practical fluency with MS Word, PowerPoint, Project, Excel, and TMF-related applications — hands-on experience with Veeva Vault or another eTMF platform is particularly valued

Preferred Qualifications:

Experience implementing and maintaining clinical applications as a business user KPI reporting; process development or writing procedural documentation Experience leading teams through change or a diverse range of working styles