Sherry Watson Email & Phone Number
@gsk.com
1 phone found area 423
LinkedIn matched
Who is Sherry Watson? Overview
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Sherry Watson is listed as Director, Global CMC Regulatory Affairs at GSK, based in Durham, North Carolina, United States. AeroLeads shows a work email signal at gsk.com, phone signal with area code 423, and a matched LinkedIn profile for Sherry Watson.
Email format at GSK
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AeroLeads found 1 current-domain work email signal for Sherry Watson. Compare company email patterns before reaching out.
About Sherry Watson
Sherry Watson is a Director, Global CMC Regulatory Affairs at GSK. She possess expertise in cmc regulatory affairs, quality by design, japan regulatory requirements, china regulatory requirements, preapproval and post approval global cmc experience and 19 more skills.
Listed skills include Cmc Regulatory Affairs, Quality By Design, Japan Regulatory Requirements, China Regulatory Requirements, and 20 others.
Sherry Watson's current company
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Sherry Watson work experience
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Director, Global Cmc Regulatory Affairs
Frequently asked questions about Sherry Watson
Quick answers generated from the profile data available on this page.
What company does Sherry Watson work for?
Sherry Watson works for GSK.
What is Sherry Watson's role at GSK?
Sherry Watson is listed as Director, Global CMC Regulatory Affairs at GSK.
What is Sherry Watson's email address?
AeroLeads has found 1 work email signal at @gsk.com for Sherry Watson at GSK.
What is Sherry Watson's phone number?
AeroLeads has found 1 phone signal(s) with area code 423 for Sherry Watson at GSK.
Where is Sherry Watson based?
Sherry Watson is based in Durham, North Carolina, United States while working with GSK.
What companies has Sherry Watson worked for?
Sherry Watson has worked for Gsk.
How can I contact Sherry Watson?
You can use AeroLeads to view verified contact signals for Sherry Watson at GSK, including work email, phone, and LinkedIn data when available.
What skills is Sherry Watson known for?
Sherry Watson is listed with skills including Cmc Regulatory Affairs, Quality By Design, Japan Regulatory Requirements, China Regulatory Requirements, Preapproval And Post Approval Global Cmc Experience, Regulatory Strategy, Global Clinical Application And Marketing Application Experience, and Agency Meeting Experience.
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