Description
IQVIA is looking for a Regulatory Affairs Manager to support regulatory activities across both Francophone and Anglophone African markets.
As a key member of our Regulatory Affairs team, you will coordinate regulatory programs, build strong relationships with clients and local partners, and help ensure successful regulatory outcomes throughout the product lifecycle.
Responsibilities
- Lead regulatory projects across multiple African markets
- Manage submission preparation, quality review, compilation and tracking activities
- Coordinate product registrations, renewals, variations and lifecycle management programs
- Work closely with local applicants, regulatory partners and health authorities
- Monitor project timelines, deliverables and risks
- Provide regulatory guidance and support to internal and external stakeholders
- Lead client governance meetings and provide regular project updates
- Maintain regulatory documentation and ensure compliance with country-specific requirements
- Contribute to delivery excellence and continuous improvement initiatives
Requirements
- Bachelor's degree in Pharmacy, Life Sciences, Medicine or a related discipline
- Minimum 5 years of Regulatory Affairs experience
- Experience supporting multiple African markets
- Strong knowledge of regulatory requirements across French-speaking and English-speaking African countries
- Experience with registrations, renewals, variations and lifecycle management activities
- Strong client-facing, communication and project management skills
- Experience managing external regulatory vendors or local partners
- Fluent French and English, written and spoken
Nice to Have
- Experience coordinating regional regulatory programs
- Experience working within a global matrix environment
- Experience supporting both Francophone and Anglophone markets
- Regulatory intelligence expertise across African markets