Research Infrastructure About Orizzonte Orizzonte Clinical Research is a UK Primary Care Site Management
Organisation operating clinical research infrastructure through research-enabled
Visit Centres embedded within established healthcare environments.
Discuss Study Delivery

About Us

Orizzonte Clinical Research is a UK Primary Care Site Management Organisation operating clinical research infrastructure through research-enabled Visit Centres embedded within established healthcare environments.

Who We Are

Orizzonte Clinical Research was established to support the delivery of clinical research through integrated healthcare environments.
The organisation operates research-enabled Visit Centres within primary care settings, creating opportunities for research delivery through established healthcare pathways while maintaining appropriate governance, quality, and operational oversight.
Our focus is on building sustainable research infrastructure that supports participants, healthcare providers, Sponsors, and CROs.

Our Vision

To lead the transformation of clinical trial delivery in the UK by integrating research into the heart of everyday healthcare, while supporting sponsors and healthcare providers with a scalable, compliant, and patient-first model.

Our Vision

We believe clinical research should be integrated into healthcare environments where appropriate, creating opportunities for broader participation and supporting research delivery closer to everyday care pathways. Our vision is to contribute to a research ecosystem where high-quality clinical research can be delivered through established healthcare environments alongside traditional research settings.

Our Vision

We believe clinical research should be integrated into healthcare environments where appropriate, creating opportunities for broader participation and supporting research delivery closer to everyday care pathways. Our vision is to contribute to a research ecosystem where high-quality clinical research can be delivered through established healthcare environments alongside traditional research settings.

Our Mission

To improve access to clinical research by embedding trials within trusted GP practices, ensuring that clinical trials are more representative, efficient, and centred around real patients in real communities.

What We Do

Orizzonte operates clinical research infrastructure designed to support study delivery across primary care environments.

Research-enabled Visit Centres
Operating dedicated and strong research sites within primary care settings to host clinical trial activities.
 Feasibility and Site Selection
Assessing study requirements and identifying suitable locations within the network to support successful trial delivery.
Study Activation and Operational Planning
Managing the setup process, including regulatory approvals, resource allocation, and site readiness.
Participant Identification Pathways
Developing and implementing strategies to connect eligible individuals with relevant research opportunities.
Study Delivery Oversight
Providing ongoing monitoring and operational support to ensure studies are conducted safely, efficiently, and in compliance with protocols.
Governance and Quality Management
Maintaining robust frameworks to uphold data integrity, participant safety, and regulatory compliance across all activities.
Sponsor and CRO Collaboration
Working closely with research sponsors and contract research organisations to align on study goals, timelines, and delivery expectations.

What We Do

Orizzonte operates clinical research infrastructure designed to support study delivery across primary care environments.

Research-enabled Visit Centres
Operating dedicated and strong research sites within primary care settings to host clinical trial activities.
 Feasibility and Site Selection
Assessing study requirements and identifying suitable locations within the network to support successful trial delivery.
Study Activation and Operational Planning
Managing the setup process, including regulatory approvals, resource allocation, and site readiness.
Participant Identification Pathways
Developing and implementing strategies to connect eligible individuals with relevant research opportunities.
Study Delivery Oversight
Providing ongoing monitoring and operational support to ensure studies are conducted safely, efficiently, and in compliance with protocols.
Governance and Quality Management
Maintaining robust frameworks to uphold data integrity, participant safety, and regulatory compliance across all activities.
Sponsor and CRO Collaboration
Working closely with research sponsors and contract research organisations to align on study goals, timelines, and delivery expectations.

Research Through Healthcare Environments

Many individuals already receive routine healthcare through GP practices and community services. Where appropriate, research activity may be delivered through these environments, helping connect clinical research with existing healthcare pathways. This approach complements traditional hospital-based research and supports a broader research delivery ecosystem.

Our Commitment to Quality

Research delivery through the Orizzonte network operates within established governance, regulatory, and quality frameworks. These frameworks support:

Participant safety
Study compliance
Data integrity
Confidentiality requirements
Operational accountability
Continuous improvement

Quality is embedded throughout the study lifecycle, from feasibility assessment through to study completion.

Working With Orizzonte

Orizzonte works with Sponsors, CROs, healthcare providers, and research partners to support clinical research delivery across primary care environments. Through research-enabled Visit Centres and coordinated operational management, the organisation supports studies across a range of therapeutic areas and delivery models.

Our Core Values

Patient-Centricity

We prioritise comfort, access, and safety in every step of the patient journey.

Partnership

We collaborate with GP practices, sponsors, and CROs to deliver meaningful research outcomes.

Innovation

We use technology and real-world data to optimise feasibility, recruitment, and trial delivery.

Integrity & Compliance

We uphold the highest standards of clinical conduct, ethics, and data protection.

Our Core Values

Healthcare Integration

Supporting research delivery within established healthcare environments where appropriate.

Quality & Accountability

Maintaining high and lofty standards of governance, compliance, and operational delivery.

Participant Focus

Supporting positive participant experiences throughout the research journey.

Collaboration

Working closely and meticulously with healthcare providers, Sponsors, CROs, and research partners.

Continuous Improvement

Strengthening research infrastructure, delivery processes, and operational capability over time.

Quality at Every Touchpoint

Quality is embedded in everything we do, from trial delivery to data management. Our processes align with all applicable UK regulations and ethical standards.

Good Clinical Practice (GCP)

All our research staff and partner practices are trained in Good Clinical Practice (GCP), ensuring trials are conducted ethically, safely, and in full regulatory compliance.

MHRA Compliance

We strictly adhere to UK Medicines and Healthcare products Regulatory Agency (MHRA) guidelines across all clinical trial activities, documentation, and reporting processes.

Data Protection & GDPR

We protect patient data with strict confidentiality, full UK GDPR and Data Protection Act compliance, and a commitment to voluntary participation.
Our Commitment to Compliance & Quality

Our Commitment to Compliance & Quality

Quality at Every Touchpoint

Quality is embedded in everything we do, from trial delivery to data management. Our processes align with all applicable UK regulations and ethical standards.

Good Clinical Practice (GCP)

All our research staff and partner practices are trained in Good Clinical Practice (GCP), ensuring trials are conducted ethically, safely, and in full regulatory compliance.

MHRA Compliance

We strictly adhere to UK Medicines and Healthcare products Regulatory Agency (MHRA) guidelines across all clinical trial activities, documentation, and reporting processes.

Data Protection & GDPR

We protect patient data with strict confidentiality, full UK GDPR and Data Protection Act compliance, and a commitment to voluntary participation.

Frequently Asked Questions

Orizzonte Clinical Research is a UK Primary Care Site Management Organisation operating clinical research infrastructure through research-enabled Visit Centres.

A Visit Centre is a research-enabled healthcare environment supporting clinical research delivery within primary care.

Orizzonte works with Sponsors, CROs, healthcare providers, research partners, and participants.

Orizzonte supports the delivery of clinical research studies through its infrastructure model and partner network.

Orizzonte currently operates through research-enabled Visit Centres across London and surrounding regions.

Let’s Start a Conversation

Whether you are a Sponsor, CRO, healthcare organisation, or potential research partner, we welcome opportunities to discuss clinical research delivery and collaboration.

Our Commitment to Compliance & Quality

Quality is embedded in everything we do, from trial delivery to data management. Our processes align with all applicable UK regulations and ethical standards.

Good Clinical Practice (GCP)
All our research staff and partner practices are trained in GCP to ensure trials are conducted safely and responsibly.

MHRA Compliance
We follow UK Medicines and Healthcare products Regulatory Agency (MHRA) guidelines for all trial-related activities and reporting.

Data Protection & GDPR
We handle patient information with the utmost care, in full compliance with the UK GDPR and Data Protection Act. Participation in any trial is always voluntary, and patient confidentiality is never compromised.

Our Team

Dr Gillian Hood

Diabetes Research Manager at Barts & the London School of Medicine and Dentistry, Queen Mary, University of London

Akash Patel

Consultant Trauma and Orthopaedic Surgeon at Royal Free London NHS Foundation Trust and Associate professor at University College London

Dr Robin Wilson

Consultant Psychiatrist at Priory Roehampton

Aderonke Adebiyi

Associate Director of Nursing Research at Royal Free London NHS Foundation Trust

Aries Maximus Ogbuokiri

Founder & Chief Operating Officer

Dr Zuhaib Keekeebhai

Lead Principal Investigator – Primary Care Trials

Dr Gillian Hood

Diabetes Research Manager at Barts & the London School of Medicine and Dentistry, Queen Mary, University of London

Akash Patel

Consultant Trauma and Orthopaedic Surgeon at Royal Free London NHS Foundation Trust and Associate professor at University College London

Dr Robin Wilson

Consultant Psychiatrist at Priory Roehampton

Aderonke Adebiyi

Associate Director of Nursing Research at Royal Free London NHS Foundation Trust

Aries Maximus Ogbuokiri

Founder & Chief Operating Officer

Dr Zuhaib Keekeebhai

Lead Principal Investigator – Primary Care Trials

Empowering clinicians to become research-active is not just about advancing science — it’s about transforming care at its core

Dr. Aries Maximus Ogbuokiri

COO

Empowering clinicians to become research-active is not just about advancing science — it’s about transforming care at its core

Dr. Aries Maximus Ogbuokiri

COO

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