Site Identification & Feasibility
Identification of suitable investigators and sites with assessments aligned to protocol requirements.
Who We Are
Your Trusted Partner for Clinical Trial Site Management in Africa
Trivida Clinical partners with investigators, research sites, sponsors, and CROs to strengthen clinical trial delivery in emerging markets. We provide end-to-end site management support, ensuring trials are conducted to international standards while remaining locally informed and operationally efficient.
With over 20 years of combined clinical research experience, our leadership team brings deep expertise across site operations, trial management, GCP compliance, and data integrity.
Site Operations & Management
Day-to-day site oversight, CRA liaison, staff training, and SOP implementation.
Patient Recruitment & Retention
Community-appropriate strategies and culturally sensitive communication approaches.
Data Quality & GCP Oversight
Source data quality checks, audit readiness, and compliance monitoring.
Site Identification
Feasibility
Site Start-Up
Regulatory Support
Site Operations
Patient Recruitment
Data Quality
GCP Oversight
Site Identification
Feasibility
Site Start-Up
Regulatory Support
Site Operations
Patient Recruitment
Data Quality
GCP Oversight
Why Trivida Clinical?
The Strategic Choice for Clinical Research in Africa
- Strong investigator and hospital networks in Nigeria: Access to teaching hospitals, private specialist clinics, and community-based research centres.
- Local operational expertise with global trial standards: We bridge global expectations with local realities across multiple therapeutic areas.
- Proven experience working with sponsors and CROs: Reduced start-up timelines, consistent site performance, and reliable patient recruitment.
- Focus on sustainable research capacity building: Training and developing the next generation of clinical research professionals.
Our Vision
Leading Site Management Organisation in Africa
To become a leading Site Management Organisation in Africa, recognised for operational excellence, data integrity, and trusted partnerships in global clinical research.
Our Mission
Enable High-Quality Clinical Research
To enable high-quality, ethical, and efficient clinical research across Nigeria and Sub-Saharan Africa by strengthening site performance, supporting investigators, and delivering reliable trial outcomes for sponsors and CROs.
Site Identification & Feasibility
Identification of suitable investigators and sites with feasibility assessments aligned to protocol requirements.
Site Operations & Management
Day-to-day site oversight, CRA and sponsor liaison, staff training, and SOP implementation.
Patient Recruitment & Retention
Community-appropriate recruitment strategies and culturally sensitive communication approaches.
Our Impact
Building Research Capacity Across Africa
Years of Experience
20+
Combined clinical research experience across sponsor, CRO, and site environments.
Geographic Coverage
3
Active operations across Nigeria, West Africa, and Sub-Saharan Africa.
Site Network
Growing
Expanding network of teaching hospitals, specialist clinics, and community research centres.
What is a Site Management Organisation (SMO)?
An SMO provides operational and administrative support to clinical research sites, ensuring trials are conducted efficiently, compliantly, and to international standards. We act as the bridge between sites, sponsors, and CROs.
Who does Trivida Clinical partner with?
We partner with investigators, research sites, sponsors, and CROs to strengthen clinical trial delivery across Nigeria and Sub-Saharan Africa.
What therapeutic areas do you support?
We support studies across infectious diseases, women's health, chronic conditions, non-communicable diseases, and public health/epidemiology.
How do you ensure GCP compliance?
We implement rigorous SOPs, conduct source data quality checks, provide GCP training, and maintain audit and inspection readiness across all managed sites.
What types of sites do you work with?
Our network includes teaching hospitals, private specialist clinics, and community-based research centres across Nigeria and Sub-Saharan Africa.
Do you support patient recruitment?
Yes, we develop community-appropriate recruitment strategies, participant engagement plans, and culturally sensitive communication approaches to meet enrollment targets.
How can sponsors and CROs benefit from working with Trivida?
We offer reduced start-up timelines, consistent site performance, strong local regulatory navigation, reliable patient recruitment, and high-quality, inspection-ready data.
Do you provide training for site staff?
Yes, we provide GCP training, protocol-specific training, and ongoing capacity development for clinical trial coordinators, research nurses, and site operations staff.
How can I join a clinical trial?
Trivida Clinical ensures all studies are conducted ethically and safely. Contact us to learn about ongoing and upcoming studies in your area.
Are you hiring?
We are building a strong clinical research workforce across Nigeria and Sub-Saharan Africa. Opportunities include Clinical Trial Coordinators, Research Nurses, Data Specialists, and Site Operations Staff. Contact us for current openings.
