O4 Research
A UK & Ireland–based clinical research and site management organisation established in 2009 that provides full-service and functional support for late-phase interventional trials and non-interventional/real-world evidence studies. Core offerings include study design and delivery, site management (on- and off-site), patient recruitment and retention, electronic data capture and data management, regulatory/ethics submissions support, clinical monitoring, medical writing and publication planning. Services are delivered for pharma, biotech and consumer health clients across multiple therapeutic areas.
Industries
Nr. of Employees
small (1-50)
O4 Research
Belfast, Northern Ireland, United Kingdom
Products
O4 Engage
A proprietary platform used to support site management, engagement, and operational continuity throughout clinical studies.
O4 Engage TM
A customized communication solution designed to secure site engagement and support patient recruitment and retention.
O4 Accelerate
A technological solution and platform deployed for robust feasibility, site selection, training, and site activation in clinical and epidemiological studies.
Accelerate TM
A proprietary study start-up optimization process used to drive enrolment phase timelines and achieve rapid site activation.
Clinical Trial Design and Management
Full-service clinical trial delivery from concept development to completion, supported by proprietary engagement methodologies.
Functional Support
Customised functional services for specific tasks required to manage and complete the drug or medical device development study life cycle.
O4 Engage
A proprietary platform used to support site management, engagement, and operational continuity throughout clinical studies.
O4 Engage TM
A customized communication solution designed to secure site engagement and support patient recruitment and retention.
O4 Accelerate
A technological solution and platform deployed for robust feasibility, site selection, training, and site activation in clinical and epidemiological studies.
Accelerate TM
A proprietary study start-up optimization process used to drive enrolment phase timelines and achieve rapid site activation.
Clinical Trial Design and Management
Full-service clinical trial delivery from concept development to completion, supported by proprietary engagement methodologies.
Functional Support
Customised functional services for specific tasks required to manage and complete the drug or medical device development study life cycle.
Services
Full-service trial design and operational delivery including protocol development, site activation and study oversight for late-phase clinical trials.
End-to-end observational study execution including study branding, patient engagement, site activation and data collection to generate RWE datasets.
Provision of managed clinical research coordinators, off-site management processes and site-level support to accelerate recruitment and maintain data quality.
Custom delivery of discrete functions across the study lifecycle including project management, site management, feasibility & start-up, recruitment, medical writing, regulatory & ethics, clinical monitoring, clinical development planning, consultancy, and data management & statistics.
Therapeutic-focused data management, CRF/eCRF and EDC design, query resolution, data reconciliation and statistical reporting to produce analysis-ready datasets.
Full-service trial design and operational delivery including protocol development, site activation and study oversight for late-phase clinical trials.
End-to-end observational study execution including study branding, patient engagement, site activation and data collection to generate RWE datasets.
Provision of managed clinical research coordinators, off-site management processes and site-level support to accelerate recruitment and maintain data quality.
Custom delivery of discrete functions across the study lifecycle including project management, site management, feasibility & start-up, recruitment, medical writing, regulatory & ethics, clinical monitoring, clinical development planning, consultancy, and data management & statistics.
Therapeutic-focused data management, CRF/eCRF and EDC design, query resolution, data reconciliation and statistical reporting to produce analysis-ready datasets.
Expertise Areas
- Clinical trial management (Phase II–IV)
- Real-world evidence and observational studies
- Site management and on-site coordinator deployment
- Patient recruitment and retention
Key Technologies
- Electronic data capture (EDC) systems
- eCRF design
- Clinical data management platforms
- Biostatistics and statistical analysis
News & Updates
Epidemiological study outputs were published in the Journal of the European Academy of Dermatology and Venereology and presented as oral and poster presentations at the EADV Congress.
Epidemiological study outputs were published in the Journal of the European Academy of Dermatology and Venereology and presented as oral and poster presentations at the EADV Congress.