Redefining Clinical Project Management: The Strategic Power of FSP Models

Biotech, Clinical Trials, Drug Discovery & Development, Life Science, Pharma,
  • Thursday, October 16, 2025 | 11am EDT (NA) / 4pm BST (UK) / 5pm CEST (EU-Central)
  • 60 min

As clinical trials continue to grow in complexity, sponsors are under increasing pressure to maintain operational control, ensure consistent quality and optimize resource allocation – all while managing costs. This webinar explores the rising demand for flexible, expert-driven project management models that empower sponsors to design and implement scalable solutions, whilst enabling them to enhance delivery performance without compromising on quality or control.

The panel explores different options available through functional service provider (FSP) partners, with a focus on the advantages of centralized project management resourcing, particularly in regions with limited access to experienced professionals. By shifting from regionalized models to centralized repositories, sponsors can better match specialized roles with the right expertise. The webinar will also highlight the importance of project management capabilities, which enable sponsors to retain closer control of study progress and enhance communication across teams.

IQVIA’s integrated support model, which combines expert project managers with centralized functions such as vendor management, document control and administrative services, can be a crucial element to get right. This structure ensures consistent delivery across all study phases, including the often-overlooked continuation and closeout stages. Dedicated teams manage data cleaning, site readiness and inspection preparedness, allowing senior staff to focus on strategic priorities.

This session is essential for clinical operations leaders seeking to elevate trial performance through smarter clinical project management. Register now to learn how IQVIA delivers scalable, high-quality solutions that meet the demands of modern clinical research.

Speakers

Ian Pemberton, IQVIA

Ian Pemberton, VP Clinical Operations, IQVIA

Ian has 28 years in clinical research and has worked in pharma companies and CROs in that time in several operational and leadership roles. Ian has spent the last 18 years working in IQVIA in Clinical, Project Management, Regulatory & Start-up roles, with the last four years leading the setup, implementation and oversight of clinical FSP models.

Message Presenter
Claire Rielly, IQVIA

Claire Rielly, VP, Hybrid Strategy and Study Management Lead, IQVIA

Claire heads the hybrid strategy for FSP and study management. Claire oversees both RSU and Clinical Project Management functions. With over 20 years of clinical experience, she has developed a broad range of experience. She began her career in clinical research in 1998 as a CRA and worked as a CRA, Clinical Lead and Line Manager in both CRO and pharma settings.

Since 2016, Claire has held leadership roles (Associate Director, Director and Senior Director) for multiple FSP accounts and became Regional Head for EMEA in 2019, driving delivery, quality, people development, financial performance and customer delivery for all FSP accounts across the region. In January 2024, she assumed her current role.

Message Presenter

Who Should Attend?

This webinar will appeal to:

  • Heads (Directors, VPs etc) of Clinical Development
  • Head (Directors, VPs etc) of Clinical Project Management
  • Global Project Lead
  • Clinical Program Directors
  • Clinical Trial Manager

What You Will Learn

Attendees will gain insights into the following topics:

Industry Shift Toward Flexibility in Project Management

  • Sponsors are adopting flexible workforce models to meet project management and oversight demands without maintaining large internal teams

Centralised Expertise for Better Fit

  • Centralizing select project management activities can unlock significant operational efficiencies, streamlining oversight and resource allocation while maintaining high standards of quality and delivery performance

Integrated Oversight Enhances Control

  • Internal project management capabilities improve trial visibility, responsiveness and sponsor control

IQVIA’s Support Model Drives Efficiency

  • Expert project managers are supported by centralized functions that streamline vendor, document and administrative management

Dedicated Trial Transition Team for Quality Delivery

  • Specialized teams manage continuation and closeout phases, ensuring clean data and site readiness while allowing senior staff to focus on new trials

Xtalks Partner

IQVIA

IQVIA (NYSE:IQV) is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. IQVIA creates intelligent connections to deliver powerful insights with speed and agility — enabling customers to accelerate the clinical development and commercialization of innovative medical treatments that improve healthcare outcomes for patients. With approximately 82,000 employees, IQVIA conducts operations in more than 100 countries. Learn more at www.iqvia.com.

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