Senior Director, Global Regulatory Affairs
Current
May 2023 - Present
AeroLeads people directory · profile
Lee Bennett Email & Phone Number
Sr Director of Global Regulatory Affairs at AstraZeneca
at
AstraZeneca
1 work email found
@astrazeneca.com
LinkedIn matched
✓ Verified Jun 2026
4 data sources
Profile completeness 100%
Current company
Role
Sr Director of Global Regulatory Affairs at AstraZeneca
Location
Gaithersburg, Maryland, United States
Who is Lee Bennett? Overview
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Quick answer
Lee Bennett is listed as Sr Director of Global Regulatory Affairs at AstraZeneca at AstraZeneca, based in Gaithersburg, Maryland, United States. AeroLeads shows a work email signal at astrazeneca.com and a matched LinkedIn profile for Lee Bennett.
Lee Bennett previously worked as Senior Director, Global Regulatory Affairs at Astrazeneca and Director of Regulatory Affairs at Astrazeneca. Lee Bennett holds Ph.D, Analytical Chemistry from Florida State University.
Company email context
Email format at AstraZeneca
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{first}.{last}@astrazeneca.com
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Profile bio
About Lee Bennett
>20 years experience in Global Pharmaceutical Company as line manager, project manager and contributor in both Regulatory Affairs and Pharmaceutical Development Analysis functions. Experienced global manager, living, working and managing projects and teams in both US and UK .Specialties: Regulatory Strategy, Project and Team Management, Pharmaceutical Development-Analysis, Project and Team Management, Risk Management, Method Development, Validation, cGMP, CMC, Regulatory Documentation, Stability, Impurities, Drug Substance and Product. Phase 1 to pre-NDA/MAA Pharmaceutical Development and CMC Authoring Experience.US native with UK work experience
Listed skills include Analytical Chemistry, Hplc, Gmp, Pharmaceutical Industry, and 27 others.
Current workplace
Lee Bennett's current company
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12 roles
Lee Bennett work experience
A career timeline built from the work history available for this profile.
Nov 2018 - May 2023
Associate Regulatory Project Director
Provide strategic input, project management and drug project support for regulatory submissions in major and emerging markets, supporting development and marketing applications, variations and maintenance submissions.
Jan 2017 - Nov 2018
Associate Regulatory Project Director
Provide strategic input, project management and drug project support for regulatory submissions in major and emerging markets, supporting development and marketing applications, variations and maintenance submissions.
Jun 2016 - Jan 2017
Associate Director & Group Manager, Regulatory Project Management
- Provide global leadership, site line management, and global drug project support. Lead global process management interactions with key customers and stakeholders. Contribute to the strategy, direction and efficient.
- Line and performance management (for Assoc Dir, PM and Regulatory Assistant levels)
- Contribute to staff and organizational learning and development
- Provide global regulatory project management and support
- Contribute to global regulatory strategy and risk management
- Contribute to global organizational strategy, development and budget
Jun 2014 - Jun 2016
Regulatory Project Manager
Secondment (temporary post) in Regulatory Affairs, Emerging Markets, Project Manager for Regulatory updates to mature products in Latin America, Asia/Pacific and Middle East/Africa markets.
Dec 2013 - Jun 2014
Team Manager, Analytical Sciences Uk
Team and Project management for analytical support of pharmaceutical development including risk assessment, lean activities method development/validation and stability/release.
Sep 2010 - Dec 2013
Team Manager, Analytical Development
Manage team performance and Pharmaceutical Development projects for analytical function. Accountable for delivery of methods, validation, release, CMC documentation and team/individual performance. Help guide development of effective and efficient process for development. Responsible for risk management within associated projects.
Apr 2009 - Sep 2010
Senior Scientist Ii
Project responsibilities for Analytical strategy development, stability, CMC documentation, risk management, substance and product development and support.
Jan 2005 - Apr 2009
Senior Scientist I
Responsible for development and validation of pharmaceutical methods, cGMP documentation and department improvement projects
Aug 2000 - Jan 2005
Graduate Research And Teaching Assistant (Research Advisor
Characterization of Organic Phosphorus Speciation in the Florida Everglades by Capillary Electrophoresis (CE) and Liquid Chromatography (HPLC) couple to Inductively Coupled Plasma-Mass Spectrometry (ICP-MS)
Aug 1994 - Jun 2000
Analytical Lab Technician
Griffin Corporation
Agrochemical sample preparation, analysis, method development and validation.
Dec 1992 - Aug 1994
3 education records
Lee Bennett education
Ph.D, Analytical Chemistry
Florida State University
Mba, Masters Of Business Administration
Wilmington University
Bs, Chemistry
Valdosta State University
FAQ
Frequently asked questions about Lee Bennett
Quick answers generated from the profile data available on this page.
What company does Lee Bennett work for?
Lee Bennett works for AstraZeneca.
What is Lee Bennett's role at AstraZeneca?
Lee Bennett is listed as Sr Director of Global Regulatory Affairs at AstraZeneca at AstraZeneca.
What is Lee Bennett's email address?
AeroLeads has found 1 work email signal at @astrazeneca.com for Lee Bennett at AstraZeneca.
Where is Lee Bennett based?
Lee Bennett is based in Gaithersburg, Maryland, United States while working with AstraZeneca.
What companies has Lee Bennett worked for?
Lee Bennett has worked for Astrazeneca, Florida State University, and Griffin Corporation.
How can I contact Lee Bennett?
You can use AeroLeads to view verified contact signals for Lee Bennett at AstraZeneca, including work email, phone, and LinkedIn data when available.
What schools did Lee Bennett attend?
Lee Bennett holds Ph.D, Analytical Chemistry from Florida State University.
What skills is Lee Bennett known for?
Lee Bennett is listed with skills including Analytical Chemistry, Hplc, Gmp, Pharmaceutical Industry, Drug Development, Method Development, Validation, and R&D.
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