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Lisa Chao Email & Phone Number

Executive Director, Global Regulatory Affairs - Oncology at Merck
Location: Hoboken, New Jersey, United States 9 work roles 1 school
2 work emails found @merck.com LinkedIn matched
✓ Verified July 2026 4 data sources Profile completeness 100%

Contact Signals · 2 work emails

Work email l****@merck.com
LinkedIn Profile matched
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Current company
Role
Executive Director, Global Regulatory Affairs - Oncology
Location
Hoboken, New Jersey, United States

Who is Lisa Chao? Overview

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Quick answer

Lisa Chao is listed as Executive Director, Global Regulatory Affairs - Oncology at Merck, based in Hoboken, New Jersey, United States. AeroLeads shows a work email signal at merck.com and a matched LinkedIn profile for Lisa Chao.

Lisa Chao previously worked as Senior Director, Global Regulatory Affairs - Oncology at Merck and Director, Global Regulatory Affairs - Oncology at Merck. Lisa Chao holds Phd, Chemistry from Mcmaster University.

Company email context

Email format at Merck

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{first}.{last}@merck.com
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AeroLeads found 2 current-domain work email signals for Lisa Chao. Compare company email patterns before reaching out.

Profile bio

About Lisa Chao

Lisa Chao is a Executive Director, Global Regulatory Affairs - Oncology at Merck. She possess expertise in regulatory affairs, drug development, clinical development, pharmaceutical industry, ind and 19 more skills.

Listed skills include Regulatory Affairs, Drug Development, Clinical Development, Pharmaceutical Industry, and 20 others.

Current workplace

Lisa Chao's current company

Company context helps verify the profile and gives searchers a useful next step.

Merck
Merck
Executive Director, Global Regulatory Affairs - Oncology
AeroLeads page
9 roles

Lisa Chao work experience

A career timeline built from the work history available for this profile.

Executive Director, Global Regulatory Affairs - Oncology

Current

Rahway, New Jersey, Us

May 2021 - Present

Senior Director, Global Regulatory Affairs - Oncology

Rahway, New Jersey, Us

Jan 2020 - May 2021

Director, Global Regulatory Affairs - Oncology

Rahway, New Jersey, Us

May 2017 - Jan 2020

Deputy Director, Global Regulatory Affairs - Oncology

Leverkusen, North Rhine-Westphalia, De

Sep 2014 - May 2017

Associate Director, Global Regulatory Affairs

Leverkusen, North Rhine-Westphalia, De

Feb 2013 - Sep 2014

Director, Regulatory Strategy - Consultant

Berkeley Heights, New Jersey, Us

Advyzom is a leading boutique consulting company specializing in highly strategic regulatory and development advice and services for partners in the pharmaceutical and healthcare industry.

Aug 2011 - Jan 2013

Senior Program Manager, Pharma Development Regulatory

Switzerland 🇨🇭 , Ch

Feb 2007 - Aug 2011

Project Manager, Discovery Project Management

Switzerland 🇨🇭 , Ch

Dec 2002 - Feb 2007

Project Manager, Research Project Management

Emeryville, California, Us

Sep 2000 - Nov 2002
1 education record

Lisa Chao education

  • Mcmaster University
    Mcmaster University
    Chemistry
FAQ

Frequently asked questions about Lisa Chao

Quick answers generated from the profile data available on this page.

What company does Lisa Chao work for?

Lisa Chao works for Merck.

What is Lisa Chao's role at Merck?

Lisa Chao is listed as Executive Director, Global Regulatory Affairs - Oncology at Merck.

What is Lisa Chao's email address?

AeroLeads has found 2 work email signals at @merck.com for Lisa Chao at Merck.

Where is Lisa Chao based?

Lisa Chao is based in Hoboken, New Jersey, United States while working with Merck.

What companies has Lisa Chao worked for?

Lisa Chao has worked for Merck, Bayer Healthcare, Advyzom, Roche Pharmaceuticals, and Chiron Corporation.

How can I contact Lisa Chao?

You can use AeroLeads to view verified contact signals for Lisa Chao at Merck, including work email, phone, and LinkedIn data when available.

What schools did Lisa Chao attend?

Lisa Chao holds Phd, Chemistry from Mcmaster University.

What skills is Lisa Chao known for?

Lisa Chao is listed with skills including Regulatory Affairs, Drug Development, Clinical Development, Pharmaceutical Industry, Ind, Drug Discovery, Regulatory Submissions, and Strategy.

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