Decrease clinical development costs and increase study quality using our global functional resources and flexible services, and get more value from your R&D spend.
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.
Centralised Expertise for Better Fit
Integrated Oversight Enhances Control
IQVIA’s Support Model Drives Efficiency
Dedicated Trial Transition Team for Quality Delivery
Ian Pemberton, VP Clinical Operations, IQVIA
Claire Rielly, VP, Hybrid Strategy and Study Management Lead, IQVIA
For more information and to register, click here.
Decrease clinical development costs and increase study quality using our global functional resources and flexible services, and get more value from your R&D spend.