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Regulatory Affairs Manager

IQVIA


Job Location:

Cairo - Egypt

Monthly Salary: Not provided by the employer
Posted: 29 August 2026 (8 days ago)
Application Deadline: 26 November 2026
Vacancies: 1 Vacancy

Job Summary

Combine regulatory expertise with strategic business impact.

IQVIA is seeking a highly experienced Global Regulatory Affairs Lead to provide regulatory leadership while supporting strategic client growth initiatives. This is a unique opportunity for a regulatory professional who enjoys both scientific and commercial conversations and who can confidently advise clients while helping develop innovative regulatory solutions.

In this highly visible role you will partner with clients business development teams and regulatory experts across multiple regions. You will shape regulatory strategies contribute to proposals and bid defenses and support the successful delivery of complex global and regional projects. The role combines regulatory leadership with significant client engagement and business development exposure.

What Youll Do

  • Lead regulatory strategy and execution for regional and global client projects Provide expert guidance on regulatory submissions lifecycle management and regulatory intelligence
  • Support proposal development bid defenses and strategic client engagements Partner with business development teams to identify and pursue growth opportunities
  • Build strong relationships with clients and act as a trusted regulatory advisor Support health authority interactions and regulatory planning activities
  • Ensure successful delivery of projects within scope timeline and quality expectations
  • Mentor colleagues and contribute to regulatory best practices
  • Drive continuous improvement initiatives across regulatory operations

What Were Looking For

  • Degree in Life Sciences or a related discipline
  • Significant Regulatory Affairs experience in global and regional environments Strong understanding of regulatory requirements across multiple markets Experience preparing and managing CTD/eCTD submissions
  • Strong client-facing and stakeholder management capabilities
  • Experience supporting proposal development business development or pre-award activities
  • Commercial awareness and the ability to identify growth opportunities
  • Strong communication presentation and influencing skills
  • Ability to work independently in a fast-paced client-focused environment
Nice to Have

  • Experience participating in bid defenses or client pitches
  • Experience supporting business development teams
  • Subject matter expertise in areas such as lifecycle management labeling publishing CMC or regulatory operations
  • Experience working in consulting CRO or client services environments

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

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.


Required Experience:

Manager


About Company

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IQVIA is the Human Data Science Company™. We are inspired by the industry we serve and provide solutions that enable life sciences companies to innovate with confidence, maximize opportunities and ultimately drive human health outcomes forward. Our approach is Human Data Science – a d ... View more

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