Requirements
Bachelor's degree in Pharmacy, Life Sciences, or Medicine with a minimum of 5 years of Regulatory Affairs experience supporting multiple African markets. Must have strong knowledge of regulatory requirements across French and English-speaking African countries, experience with registrations, renewals, variations, and lifecycle management. Excellent client-facing, communication, and project management skills are essential, along with experience managing external regulatory vendors or local partners. Fluency in both written and spoken French and English is required.
Description
Lead regulatory programs across Africa and make a meaningful impact on patient access.IQVIA is looking for a Regulatory Affairs Manager to support regulatory activities across both Francophone and Anglophone African markets. This role combines regulatory expertise, project leadership and client engagement, offering the opportunity to work across diverse healthcare environments and support product registrations across multiple countries.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.What You'll DoLead regulatory projects across multiple African marketsManage submission preparation, quality review, compilation and tracking activitiesCoordinate product registrations, renewals, variations and lifecycle management programsWork closely with local applicants, regulatory partners and health authoritiesMonitor project timelines, deliverables and risksProvide regulatory guidance and support to internal and external stakeholders Lead client governance meetings and provide regular project updatesMaintain regulatory documentation and ensure compliance with country-specific requirementsContribute to delivery excellence and continuous improvement initiativesWhat We're Looking ForBachelor's degree in Pharmacy, Life Sciences, Medicine or a related disciplineMinimum 5 years of Regulatory Affairs experienceExperience supporting multiple African marketsStrong knowledge of regulatory requirements across French-speaking and English-speaking African countriesExperience with registrations, renewals, variations and lifecycle management activitiesStrong client-facing, communication and project management skillsExperience managing external regulatory vendors or local partnersFluent French and English, written and spokenNice to HaveExperience coordinating regional regulatory programsExperience working within a global matrix environmentExperience supporting both Francophone and Anglophone marketsRegulatory intelligence expertise across African marketsIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.comIQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.