Regulatory Affairs Manager — West Africa
Lead dossier strategy and submissions across ECOWAS/UEMOA markets. Several years’ NRA submission experience required.
Dakar or Abidjan
Careers
Help get safe medicines to African patients — faster.
We’re building the regulatory partner Africa’s pharmaceutical market needs. If you want your expertise to have real impact on access to medicines, we want to talk to you.
Why work with us
Real submissions. Real markets. Real ownership.
You’ll work across multiple African markets and frameworks, alongside experienced practitioners, on real submissions and systems rather than abstractions.
We value precision, ownership, and clear thinking, and we invest in our people through ProReg Academy and hands-on mentorship. We bring together physicians, regulatory affairs specialists, pharmacovigilance experts, and clinical research professionals — with a direct, output-focused, accountable culture.
Open roles
Where we’re hiring.
Pharmacovigilance Officer / Local QPPV
Operate PV systems and serve as local PV contact for client products. PV case processing and reporting experience required.
Cameroon
Regulatory Affairs Officer — Central Africa
Support registrations and lifecycle maintenance across CEMAC markets. Early-career candidates welcome.
Yaoundé / Douala
Clinical Trials & Ethics Submissions Specialist
Manage ethics and regulatory submissions, IMP import permits, and GCP readiness for studies in the region.
Flexible, West/Central Africa
Roles shown are illustrative — we review applications on a rolling basis and respond to every candidate.
How to apply
Send your CV and a short note on the role and markets that interest you.
careers@proregafrica.com