Our Individual Resourcing solution provides access to skilled research and clinical trial professionals on an as-needed basis, allowing Sponsors, CROs, and Sites to fill critical roles without long-term commitments. Our powerful recruiting engine efficiently identifies the right person for the job. Since the candidates become Vitalief employees, we have a vested interest in their success. This model offers:

• Skilled Resources
  Deploy skilled professionals as needed to support key functions across research and clinical trial operations, ensuring flexibility, continuity, and performance where it's needed most.
• On-Demand Flexibility
  Scale your team up or down based on current trial needs, maintaining efficiency while controlling costs.
• Institutional Confidence
  Our clients can trust that every professional we provide is not only carefully selected through our efficient and proven talent acquisition process but is also fully supported by the collective expertise and resources of our entire organization. This ensures they have the support and backing needed to succeed in their roles.

DIRECT HIRE
We also offer direct hire services that connect sponsors, CROs, and Sites with top-tier talent for full-time roles across clinical operations, regulatory affairs, data management, and more. We manage the full recruitment lifecycle, from sourcing and screening to offer negotiation, ensuring a seamless process and a strong fit for both the organization and candidate. Our industry expertise and deep talent network help you build high-performing teams quickly, reducing time-to-hire and enhancing long-term success.

Our Managed Services provide dedicated teams to oversee and execute specific tasks or functions end-to-end, while our Shared Services offer flexible, scalable support across multiple functions, shared among projects to maximize efficiency and resource allocation. This dual approach allows sites to allocate resources effectively while ensuring quality and compliance. Our services include but are not limited to the following:

• Clinical Trial Billing and Financial Management
  Complete oversight of budget analysis, billing, reconciliation, and invoicing to maintain financial accuracy and efficiency.
• Operational and Regulatory Management
  Support for essential tasks like IRB submissions, quality assurance, and day-to-day trial operations, ensuring that trials remain compliant and on schedule.
• Flexible Shared Resources
  Access to resources across multiple functions, including project management, data management, and document handling, allowing for resource sharing based on project needs.

Vitalief’s FSP solutions offer a strategic approach to outsourcing, combining industry expertise with flexible service models that optimize operations and support trial success. Our commitment to quality, efficiency, and compliance makes us a trusted partner in research and clinical trials, providing the support Sponsors, CROs, and Sites need to manage resources effectively and deliver high-quality outcomes.

Vitalief delivers integrated solutions for sponsors, CROs, and clinical trial sites that improve operational efficiency, enhance study performance, and address resourcing and strategic challenges across the research and clinical trial ecosystem.

Interested in optimizing your clinical trial operations? Connect with our Subject Matter Experts to explore tailored strategies that drive efficiency, compliance, and measurable results.