- Per protocolStaff selected against each study's requirements
- Every phaseCoordinators, nurses, data and lab staff
- Nigeria-wideLagos and other sites, agreed at scoping
Built around your protocol.
For sponsors, CROs, hospitals and academic groups running trials across maternal and child health, infectious diseases, oncology, cardiovascular, diabetes, mental health and vaccines.
What a visit looks like
From protocol to study team
Timelines are agreed at scoping and depend on the protocol.
- Scoping
Your protocol
Roles, sites, training and regulatory requirements.
- Selection
Matched staff
Selected against the protocol's stated requirements.
- Checks
Evidence confirmed
GCP training and regulatory briefing confirmed per study.
- Deployment
On site
Teams start at your sites on the agreed date.
- Ongoing
Support
Coordination and adjustments for the life of the study.
Who we put on your study
Selected against your protocol.
- Identity checked
- Credentials checked
- GCP training evidenced per study
- Regulatory briefing confirmed
- References taken
- Matched to the protocol
Quoted per scope
Tell us about the study
Research staffing is quoted per protocol. A coordinator calls you back to scope roles, sites and timelines.
How it starts
From first message to first visit
- 1
Share the study
Protocol, sites, roles and timelines.
- 2
Scoping
We agree requirements and a deployment timeline.
- 3
Selection
Staff matched and evidence confirmed per study.
- 4
Deployment
Teams on site, with ongoing support.
Share the study
Protocol, sites, roles and timelines.
If something changes
Your worries, answered
- “Are your staff GCP compliant?”Evidence of GCP training and regulatory briefing is confirmed per study.
- “How quickly can you staff a site?”Timelines are agreed at scoping, by protocol and geography.
- “Do you work outside Lagos?”Yes, across Nigerian sites, agreed at scoping.
- “What therapeutic areas?”Maternal and child health, infectious disease, oncology, cardiovascular, diabetes, mental health and vaccines.
Evidence of GCP training and regulatory briefing is confirmed per study.
Questions
More questions
Are you a Clinical Research Organisation (CRO) in Nigeria?
Medic Connect is a clinical research staffing and support partner based in Lagos. We supply coordinators, research nurses, data managers and lab staff to CROs, sponsors, hospitals and academic institutions running trials in Nigeria, matched to each protocol's stated requirements.
What therapeutic areas do you cover?
Our research workforce supports trials across maternal & child health, infectious diseases (including HIV, TB and malaria), oncology, cardiovascular, diabetes, mental health and vaccine studies.
Are your research staff GCP and NAFDAC compliant?
Research personnel are selected against the protocol's stated training and regulatory requirements, and evidence of GCP training and regulatory briefing is confirmed per study. We can deploy across Lagos and other Nigerian states.
How quickly can you staff a clinical trial site?
Deployment timelines are agreed at scoping and depend on protocol complexity, geography and required certifications.
Staff your next study.
Tell us about the protocol and we will scope the team.