End-to-end Site Operations

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Your study. Our sites. Full operational delivery.

Pratia provides full operational leadership at the site level, taking clear ownership and responsibility for study delivery from start-up through close-out.

Through our dedicated research sites and embedded hospital units, we manage the day-to-day execution of clinical trials across a wide range of therapeutic areas, allowing Sponsors and CROs to work with one experienced partner throughout the site journey.

In simple terms: You provide the study requirements. We provide the site-level research operations, dedicated team and operational oversight needed to deliver it.

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From start-up to close-out

Whether for early-phase research, larger-scale Phase II–IV studies or decentralized trials, Pratia provides end-to-end solutions covering:

Feasibility and Study Start-Up

Comprehensive site assessments, contracting and staff training to ensure an efficient trial launch.

Patient Recruitment and Retention

Access to a broad patient base with informed consent and retention strategies designed to support patient satisfaction and study success.

Trial Conduct and Data Collection

Protocol-based clinical study conduct, including patient reimbursement, secure IP management and real-time data entry to maintain accuracy and compliance.

Study Close-Out and Compliance

Final patient visits, data verification, regulatory documentation and audit readiness.

One service. Tailored site delivery.

Clinical trials have diverse requirements, which is why we don't rely on a single site format. Our Mixed Site Model matches your protocol with the optimal blend of research infrastructure, specialist care, and patient access across Europe and the US.

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Dedicated Site Model

Pratia-operated research environments designed for efficient clinical trial delivery and patient recruitment. Includes our standalone outpatient clinics, 5 exclusive oncology units across three countries, and our specialized 40-bed First-in-Human / Early Phase facility. We provide experienced research teams and established operational processes to support high-quality, protocol-compliant study conduct.

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Embedded Site Model

Pratia research operations integrated directly within host hospitals. We embed our own study teams, management, and operational processes inside existing hospital systems. Our teams use the hospital’s established infrastructure and clinical facilities while Pratia manages research operations, patient recruitment, and study delivery.

Additional capabilities when your study needs them

Beyond site management, we provide specialized end-to-end expertise to support complex protocol requirements:

Clinical & Non-Clinical Strategy Consulting

Medical Writing: protocol, ICF, CRF

Pharmacokinetics & Biostatistics

Biosampling

Why choose End-to-End Site Operations?

The best operational model for your study

Our Mixed Site Model allows us to select the environment that best fits your protocol, patient population, therapeutic area and infrastructure requirements.

Patient-Centric clinical trials at scale

We deliver high-quality feasible Patient-Centric clinical trials on a global scale, supported by our network of sites across Europe.

A platform for innovative medicine

We provide patients with access to innovative treatment options in a high-quality research environment, supported by close collaboration with local healthcare systems.

Broad therapeutic coverage

Our network can support studies across a broad range of therapeutic areas, with the ability to cover on average 85% of all indications.

Flexible study delivery

We can adapt to the changing requirements of the clinical research industry, including Remote Monitoring and Decentralized Studies.

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A network built for clinical trial delivery

Our scale, therapeutic expertise and established site network allow us to support Sponsors and CROs across diverse study requirements and patient populations.

100 sites - across 8 countries, offering tailored mixed-site solutions to match your protocol and recruitment targets for Phase II–IV trials.

85% indication coverage - broad therapeutic reach based on recent market research and RFIs.

Over 35% oncology experience - deep specialized expertise backed by 5 exclusive oncology units across 3 countries and multiple embedded hospital sites.

Trust is the foundation of every successful partnership.

Our strength lies in understanding our clients’ challenges and working collaboratively to deliver tailored solutions that accelerate clinical development.

Portrait of Chloe Rose

Chloe Rose

Vice President, Site Solutions

Centralized support. Local site delivery.

We reduce administrative complexity by centralizing project oversight and commercial operations across the site network.

Feasibility & Commercial

Fast turnaround on RFIs, Yes/No decisions, Country/Site/Patient (CSP) mixes, and fully costed proposals. All feasibility is subject to scientific input from our investigators, heavily reducing post-award site dropouts.

Project & Relationship Management

One coordinated view of study progress. A dedicated Global Project Management team facilitates communication between sites and sponsor/CRO teams, tracks milestone delivery, and expedites study startup.

Contracting

One contract (CTA or Work Order under an existing MSA) is all that is needed – regardless of the volume of sites and vendors. Includes ONE budget per country, ONE Schedule of work globally and ONE invoice each month.​

From first conversation to full site delivery

  • Contact us

  • Let's discuss your project

  • Receive your tailored proposal

  • Get your study moving

Looking for end-to-end site delivery?

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Frequently Asked Questions

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