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Availability & Opportunities

Mobilize qualified resources for your clinical trials in Francophone Africa

AFCRA facilitates the identification and mobilization of qualified resources in clinical research and allows professionals and investigation sites to express their interest in future collaborations.

Who is this service for?
A system for all stakeholders in clinical research
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Sponsors & CROs

You need qualified and operational resources for your projects in Francophone Africa.

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Investigation sites

Your site would like to be identified, evaluated or supported for future clinical trials.

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Research professionals

Are you a freelance or professional ARC/CRA and would like to be contacted for future opportunities?.

Provision
Available profiles & AFCRA interventions

👥 Relevant profiles

  • 🔬 ARC / CRA (Clinical Research Associates)
  • 📋 Study Coordinators
  • 🏥 Clinical Research Assistants / Technicians (CRT)
  • 👨‍💼 Clinical Research Support Staff

✅ What AFCRA does

  • ✅ Identification and mobilization of qualified resources according to the project's needs
  • ✅ Provision of operational staff
  • ✅ Supervision, support and quality monitoring provided by AFCRA
Opportunities
Express your interest

👩‍🔬 For professionals

Are you a freelance CRA/CRA or clinical research professional and would like to be contacted for future opportunities in French-speaking Africa?

I am an ARC/CRA — Express my interest →

🏥 For investigative websites

Does your site wish to be identified, evaluated or supported for future clinical trials in French-speaking Africa?

I am a website — Express my interest →
What you earn
The benefits of the AFCRA scheme

Resources immediately operational

Qualified profiles, supervised and monitored by AFCRA for rapid onboarding.

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Better match between profiles and needs

Resources selected according to your specific field needs for maximum efficiency.

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Quality and compliance ensured

AFCRA provides supervision and quality monitoring throughout the entire provision process.

Our other services
Complete your support
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Site Management SMO

Operational management and structuring of investigation sites.

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Regulatory & Ethical Support

Submissions, file tracking and regulatory compliance.

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Clinical Research Training

Practical training adapted to the French-speaking African context.

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Need qualified resources or wish to express your interest?

Contact us — we'll get back to you quickly.