IQVIA Posted October 14, 2026

Regulatory Affairs Manager, Africa

New Cairo, Egypt Full time
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IQVIA is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

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 Do

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

What We're Looking For

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

IQVIA 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.com

IQVIA 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.

Job details

Seniority
Manager
Function
Clinical Development
Therapeutic area
Not listed
Location
New Cairo, Egypt
Employment type
Full time

How this role compares

Computed from every other active Clinical Development role in our database, not just this employer's listings.

We currently track 391 comparable Manager Clinical Development roles across 68 biopharma companies.

391Comparable roles tracked
367Currently active
68Companies hiring similar roles
41Countries represented

Salary context

121 of 391 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Highest disclosed · Statistical Advisor · Gilead Sciences, Inc. $226,185/yr – $292,710/yr
Peer group range $95,500 – $259,448 (median $180,500)

Where these roles are based

Top locations among the 391 comparable roles

United States182
India48
United Kingdom24
Poland13
China12
Spain11

+ 35 more countries

Seniority mix

391 of 391 peers have a known seniority level

Manager249
Associate Director112
Associate30

Therapeutic area mix

37 of 391 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology18
Immunology11
Neuroscience3
Ophthalmology2
Dermatology & Aesthetics1
Rare Disease1
Respiratory1

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The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

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Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

45%
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Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.