Elizabeth Milton
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Elizabeth Milton Email & Phone Number

Clinical Research Regulatory Specialist at University of California, San Francisco
Location: San Mateo, California, United States 10 work roles 3 schools
1 work email found @ecog-acrin.org LinkedIn matched
✓ Verified July 2026 4 data sources Profile completeness 86%

Contact Signals · 1 work email

Work email e****@ecog-acrin.org
LinkedIn Profile matched
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Role
Clinical Research Regulatory Specialist
Location
San Mateo, California, United States
Company size

Who is Elizabeth Milton? Overview

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Quick answer

Elizabeth Milton is listed as Clinical Research Regulatory Specialist at University of California, San Francisco, a with 2 employees, based in San Mateo, California, United States. AeroLeads shows a work email signal at ecog-acrin.org and a matched LinkedIn profile for Elizabeth Milton.

Elizabeth Milton previously worked as Associate Project Coordinator at Ecog-Acrin Cancer Research Group and Protocol Associate III at Ecog-Acrin Cancer Research Group. Elizabeth Milton holds Master'S Degree, Clinical Social Work from Boston University.

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Email format at University of California, San Francisco

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{first_initial}{last}@ecog-acrin.org
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AeroLeads found 1 current-domain work email signal for Elizabeth Milton. Compare company email patterns before reaching out.

Profile bio

About Elizabeth Milton

I am an experienced clinical project coordinator with a strong background in mental health and oncology research. Skilled in cross-functional collaboration with a proven ability to lead teams, manage partnerships, and manage multiple studies and projects.

Current workplace

Elizabeth Milton's current company

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University of California, San Francisco
University Of California, San Francisco
Clinical Research Regulatory Specialist
San Mateo, CA, US
Employees
2
AeroLeads page
10 roles

Elizabeth Milton work experience

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

Associate Project Coordinator

Current

Boston, Massachusetts, United States

- Manage the administrative operations for multiple clinical trials and outcomes research studies in a fast-paced, deadline-driven environment.- Coordinate timelines and milestones for clinical programs, ensuring adherence to ICH-GCP guidelines and timely execution of study goals.- Oversee clinical document management, including protocols, informed consent forms (ICFs), and manuals, ensuring clarity, regulatory compliance, and protocol quality.- Lead cross-functional collaboration with teams including the TST/biomarker team, physicians, and regulatory affairs to deliver high-quality study design and data.- Work with sites to identify potential protocol risks and develop mitigation strategies to address issues, ensuring project goals are proactively achieved.- Track and communicate study progress to senior management, developing detailed dashboards and trackers to ensure transparency and alignment on milestones.- Train and mentor junior staff, contributing to professional development and performance feedback.- Write and maintain work instructions and SOPs.

Feb 2024 - Present

Protocol Associate Iii

Boston, Massachusetts, United States

- Managed multiple clinical research studies, coordinating with cross-functional teams to meet timelines and deliverables.- Collaborated with cross-functional teams to ensure successful project outcomes, troubleshooting study issues to maintain data quality and comply with study protocols.- Utilized Microsoft Office Suite for organizing project information and tracking progress on clinical trials.- Assessed and managed issue and change requests throughout the clinical trial process, collaborating on mitigation strategies to ensure projects stayed on track. Collaborated with senior leaders to escalate when necessary.- Balanced multiple projects across various geographic regions, ensuring seamless execution and timely completion.

Dec 2022 - Feb 2024

Protocol Associate Ii

Boston, Massachusetts, United States

- Managed multiple clinical research studies, coordinating with cross-functional teams to meet timelines and deliverables.- Collaborated with cross-functional teams to ensure successful project outcomes, troubleshooting study issues to maintain data quality and comply with study protocols.- Utilized Microsoft Office Suite for organizing project information and tracking progress on clinical trials.- Assessed and managed issue and change requests throughout the clinical trial process, collaborating on mitigation strategies to ensure projects stayed on track. Collaborated with senior leaders to escalate when necessary.- Balanced multiple projects across various geographic regions, ensuring seamless execution and timely completion.

Dec 2021 - Dec 2022

Protocol Associate I

Boston, Massachusetts, United States

- Managed multiple clinical research studies, coordinating with cross-functional teams to meet timelines and deliverables.- Collaborated with cross-functional teams to ensure successful project outcomes, troubleshooting study issues to maintain data quality and comply with study protocols.- Utilized Microsoft Office Suite for organizing project information and tracking progress on clinical trials.- Assessed and managed issue and change requests throughout the clinical trial process, collaborating on mitigation strategies to ensure projects stayed on track. Collaborated with senior leaders to escalate when necessary.- Balanced multiple projects across various geographic regions, ensuring seamless execution and timely completion.

Jul 2021 - Dec 2021

Research Assistant

Boston, Massachusetts, United States

- Collected and analyzed data for studies on patient care access, utilizing statistical software such as R to conduct data cleaning and aggregation.- Analyzed descriptive statistics to identify trends in patient behavior and outcomes- Collected data from patient health profiles in accordance with HIPAA- Organized variables from raw data; analyzed physician notes, medication lists, labs, and visit notes

May 2021 - Jul 2021

Services Intern

Boston, Massachusetts, United States

- Conducted public health research, contributing to reports on state drug policy and client behavioral progress.- Designed and implemented evaluation frameworks for program effectiveness, ensuring data-driven decision-making.- Empowered college students to thrive while balancing mental health and returning to school

Aug 2020 - May 2021

School Social Work Intern

Dorchester, Massachusetts, United States

Aug 2019 - May 2020
3 education records

Elizabeth Milton education

FAQ

Frequently asked questions about Elizabeth Milton

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

What company does Elizabeth Milton work for?

Elizabeth Milton works for University of California, San Francisco.

What is Elizabeth Milton's role at University of California, San Francisco?

Elizabeth Milton is listed as Clinical Research Regulatory Specialist at University of California, San Francisco.

What is Elizabeth Milton's email address?

AeroLeads has found 1 work email signal at @ecog-acrin.org for Elizabeth Milton at University of California, San Francisco.

Where is Elizabeth Milton based?

Elizabeth Milton is based in San Mateo, California, United States while working with University of California, San Francisco.

What companies has Elizabeth Milton worked for?

Elizabeth Milton has worked for University Of California, San Francisco, Ecog-Acrin Cancer Research Group, Massachusetts General Hospital, Boston University Center For Psychiatric Rehabilitation, and Up Education Network.

How can I contact Elizabeth Milton?

You can use AeroLeads to view verified contact signals for Elizabeth Milton at University of California, San Francisco, including work email, phone, and LinkedIn data when available.

What schools did Elizabeth Milton attend?

Elizabeth Milton holds Master'S Degree, Clinical Social Work from Boston University.

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