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Andrew Dorman Email & Phone Number

Senior Director, Clinical Program Lead (Hematology and KAT6) at Stemline Therapeutics
Location: East Brunswick, New Jersey, United States 12 work roles 3 schools
1 work email found @celgene.com LinkedIn matched
✓ Verified May 2026 4 data sources Profile completeness 100%

Contact Signals · 1 work email

Work email a****@celgene.com
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Current company
Role
Senior Director, Clinical Program Lead (Hematology and KAT6)
Location
East Brunswick, New Jersey, United States

Who is Andrew Dorman? Overview

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Quick answer

Andrew Dorman is listed as Senior Director, Clinical Program Lead (Hematology and KAT6) at Stemline Therapeutics, based in East Brunswick, New Jersey, United States. AeroLeads shows a work email signal at celgene.com and a matched LinkedIn profile for Andrew Dorman.

Andrew Dorman previously worked as Senior Director, Hematology Clinical Program Lead at Stemline Therapeutics and Director, Sr. Operations Portfolio Lead at Bristol Myers Squibb. Andrew Dorman holds Dual Bachelors Of Science, Biological Sciences, Marine Science from Rutgers University.

Company email context

Email format at Stemline Therapeutics

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{first_initial}{last}@celgene.com
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AeroLeads found 1 current-domain work email signal for Andrew Dorman. Compare company email patterns before reaching out.

Profile bio

About Andrew Dorman

Knowledgeable and dedicated to oncology trials. Unwavering commitment to patients and to seeing trials through.• Over 18 years of Clinical Research experience• Over 16 years of Clinical Project Management experience• Over 16 years of Hematology (AML, MDS, CMML, Lymphoma) & Oncology (combined pediatric, brain & solid tumor, rare tumors, gastric, lung, liver, bladder, and penile) experience • Over 16 years of experience managing Oncology budgets • Over 16 years of experience managing Global trials (North America, Europe, Asia Pacific, South America, Africa, etc.); experience managing up to 24 countries at one time • Over 14 years of protocol development experience• Experience creating monitoring plans, pediatric implementation plans, informed consent documents and pediatric assent forms, case report forms and completion guidelines, subject recruitment plans, vendor oversight plans, and transition plans• Over 17 years of experience managing third party vendors (Labs, CROs, Imaging, Recruitment, Patient Travel Service, etc.)• Experience overseeing Data Management, Monitoring, and Vendor Management; experience interfacing with Regulatory, Finance, Drug Supply, Contracts & Outsourcing, Programming, and Statistics• Over 16 years of experience reviewing and developing Case Report Forms (performance scales, modifications to target lesions and non-target lesion pages, biomarker data collection, etc.) and EDC systems• Experience setting up and presenting at over 30 Investigator Meetings

Listed skills include Clinical Trials, Gcp, Clinical Data Management, Pharmaceutical Industry, and 40 others.

Current workplace

Andrew Dorman's current company

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Stemline Therapeutics
Stemline Therapeutics
Senior Director, Clinical Program Lead (Hematology and KAT6)
East Brunswick, NJ, US
AeroLeads page
12 roles

Andrew Dorman work experience

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

Senior Director, Clinical Program Lead (Hematology And Kat6)

East Brunswick, NJ, US

Senior Director, Hematology Clinical Program Lead

Current

New York, New York, US

Nov 2022 - Present

Director, Sr. Operations Portfolio Lead

Lawrence Township, NJ, US

Aug 2020 - Nov 2022

Assoc. Director, Clinical Operations Lead

Lawrence Township, NJ, US

Nov 2019 - Aug 2020

Associate Director, Clinical Trial Management

Summit, New Jersey, US

Provide strategic operational direction and execution of hematology and CAR-T clinical trials and oversight of multiple cross-functional study teams and CROs. Overall accountability for the execution of the Operations strategy for the program.Responsibility for oversight, mentoring, and training of clinical trial managers and associatesProgram oversight of.

Oct 2016 - Nov 2019

Senior Manager, Senior Clinical Trial Manager

Summit, New Jersey, US

Management of Phase I to Phase III Hematology/Oncology Trials focused on AML and MDSGlobal Lead SM on two Phase III registration trials (20+ countries; 80M+ budgets)Full CRO OversightFull Vendor OversightManagement of Regional Study Management TeamsManagement of Pediatric HemOncology Trials in AML

Nov 2012 - Sep 2016

Senior Global Study Manager

King Of Prussia, PA, US

Management of phase I, II, and III oncology trials in pediatric tumors, brain & solid tumors, rare tumors, gastric, and lung. Responsible for management of Pediatric Oncology trials. Served as Pediatric Oncology Subject Matter Expert.Served as Rare tumors Subject Matter Expert.Liaised with Pediatric Oncology Groups.Led Continuous Improvement Group Task.

Oct 2007 - Oct 2012

Global Study Manager

New York, New York, US

Management of phase I, II, and III oncology trials in pediatric tumors, brain & solid tumors, rare tumors, liver, bladder, and penile.Management of phase III, IIIb, and IV COX-2 trials (through 2005).Responsible for sponsored Pediatric Oncology trials.Liaised with pediatric cancer cooperative groups.Established and maintained Pfizer's relationship with.

Jun 2004 - Oct 2007

Imaging Repository Lead

Tampa, FL, US

Responsible for complete oversight of clinical trial image repository.Managed imaging and data entry vendors.Supervised Data Processing team and delegated all clinical team requests.

Sep 2002 - Jun 2004

Clinical Information Specialist Via Joulé Staffing

Kenilworth, New Jersey, US

Responsible for management of key regulatory documents.Coded clinical data into clinical database.

May 2002 - Aug 2002

Technical Support Associate

Miami, Florida, US

Provided technical support for company's own proprietary vitamin management, inventory, and sales software.

Jan 2001 - Apr 2002

Lab Technician

Rutgers University, Institute Of Marine And Coastal Sciences, Benthic Ecology Lab

Responsible for taxonomic review and assessment of biodiversity and biomass of microfauna in southern NJ salt marshes and neighboring benthic habitats in the Delaware bay and nearby estuaries.

Sep 1998 - Jan 2001
3 education records

Andrew Dorman education

Dual Bachelors Of Science, Biological Sciences, Marine Science

Rutgers University

Coursework Only, Project Management

Stevens Institute Of Technology

Certificate, Project Management

University Of Virginia Darden School Of Business
FAQ

Frequently asked questions about Andrew Dorman

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

What company does Andrew Dorman work for?

Andrew Dorman works for Stemline Therapeutics.

What is Andrew Dorman's role at Stemline Therapeutics?

Andrew Dorman is listed as Senior Director, Clinical Program Lead (Hematology and KAT6) at Stemline Therapeutics.

What is Andrew Dorman's email address?

AeroLeads has found 1 work email signal at @celgene.com for Andrew Dorman at Stemline Therapeutics.

Where is Andrew Dorman based?

Andrew Dorman is based in East Brunswick, New Jersey, United States while working with Stemline Therapeutics.

What companies has Andrew Dorman worked for?

Andrew Dorman has worked for Stemline Therapeutics, Bristol Myers Squibb, Celgene, Execupharm On Assignment At Pfizer, Inc., and Pfizer, Inc..

How can I contact Andrew Dorman?

You can use AeroLeads to view verified contact signals for Andrew Dorman at Stemline Therapeutics, including work email, phone, and LinkedIn data when available.

What schools did Andrew Dorman attend?

Andrew Dorman holds Dual Bachelors Of Science, Biological Sciences, Marine Science from Rutgers University.

What skills is Andrew Dorman known for?

Andrew Dorman is listed with skills including Clinical Trials, Gcp, Clinical Data Management, Pharmaceutical Industry, Clinical Development, Cro, Edc, and Therapeutic Areas.

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