Global Regulatory Affairs Manager
تفاصيل الوظيفة
Job Summary
Join IQVIA and help shape the future of global healthcare. As a Global Regulatory Affairs Manager you will ensure compliance and accelerate access to therapies across international markets.
What You Will Do
- Develop and implement regulatory strategies for assigned products in partnership with global teams and local affiliates.
- Manage submissions approvals and lifecycle activities to meet timelines and regulatory requirements.
- Act as the key liaison between global regulatory teams and affiliates ensuring alignment on priorities and documentation.
- Monitor regulatory changes and provide strategic guidance to internal stakeholders.
- Support health authority interactions including briefing documents and response planning.
What You Will Bring
- Degree in Pharmacy or Life Sciences.
- Experience in regulatory affairs across international markets.
- Strong communication and collaboration skills.
- Proficiency in regulatory systems such as Veeva RIM.
- A proactive solution-oriented mindset.
Why IQVIA
Your potential has no limits here. We thrive on innovation collaboration and a shared mission to advance healthcare worldwide. Join us and make an impact that matters.
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
Required Experience:
Manager
Key Skills
- Proofreading
- Adobe Acrobat
- FDA Regulations
- Manufacturing & Controls
- Biotechnology
- Clinical Trials
- Research & Development
- GLP
- cGMP
- Product Development
- Chemistry
- Writing Skills
Apply Now
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