We deliver integrated solutions that address the full spectrum of research and clinical trial needs - strategically, operationally, and administratively. Whether you're a Sponsor, CRO, or Site, our services are designed to reduce complexity, enhance collaboration, and drive measurable results.

From long-term strategic planning and hands-on clinical operations to administrative support, project oversight, and workforce solutions, our expert teams bring the structure, scalability, and insight needed to accelerate research and improve outcomes. 

Explore our five core service categories below to see how we can support your organization’s success.

Vitalief’s Strategic Planning services help Sponsors, CROs, and Sites define a clear path forward in an increasingly complex research environment. We co-develop multi-year strategic roadmaps, conduct trial portfolio assessments, and align resources with organizational goals.

By combining deep industry expertise, business acumen, and data-driven insights, we help clients anticipate challenges, allocate resources wisely, and position themselves for sustainable growth. The result is increased agility, more effective collaboration, and stronger performance across the organization.

Our Clinical Operations services enable faster, more reliable trial execution from start-up through closeout. We support key functions such as feasibility, trial activation, site management, quality assurance, and trial rescue, ensuring studies launch on time, stay compliant, and meet recruitment goals.

We reduce delays, elevate data quality, and improve patient access by optimizing coordination between Sponsors, CROs, and Sites. Clients gain not just operational support but a partner that proactively resolves barriers to success.

We provide the financial and regulatory infrastructure that keeps trials running efficiently and compliantly.

Our Clinical Research Administration services cover budget development and negotiation, research billing compliance, grant administration, IRB submission management, and contract oversight.

By streamlining these critical functions, we reduce administrative burden, accelerate timelines, and minimize financial and regulatory risk. Sponsors, CROs, and Sites benefit from cleaner processes, clearer documentation, and stronger fiscal control.

Vitalief delivers expert leadership to guide clinical research projects and programs from planning through completion. We design and manage PMOs, oversee multi-study programs, and provide day-to-day project management to ensure accountability, cross-functional coordination, and timely delivery.

With a structured yet flexible approach, we help research and clinical trial teams navigate complexity, mitigate risk, and stay aligned with strategic goals. The result: improved transparency, smoother execution, and greater confidence in meeting trial milestones.

Our Workforce and Talent Solutions connect Sponsors, CROs, and Sites with skilled professionals and high-performing teams tailored to their needs. Whether through embedded resources, managed services, or direct hire placements, we offer flexible staffing models that support continuity, scale, and performance.

Every resource is backed by Vitalief’s subject matter experts, training programs, and quality oversight, helping clients build lasting capabilities that go above and beyond traditional organizational boundaries to raise the bar across the entire ecosystem.