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Mary Kushman, Ph.D., M.P.H. Email & Phone Number

Toxicology Branch Chief at FDA
Location: Rockville, Maryland, United States 15 work roles 5 schools
1 work email found @fda.gov LinkedIn matched
✓ Verified August 2026 4 data sources Profile completeness 100%

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Current company
FDA
Role
Toxicology Branch Chief
Location
Rockville, Maryland, United States
Company size

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Mary Kushman, Ph.D., M.P.H. is listed as Toxicology Branch Chief at FDA, a with 14770 employees, based in Rockville, Maryland, United States. AeroLeads shows a work email signal at fda.gov and a matched LinkedIn profile for Mary Kushman, Ph.D., M.P.H..

Mary Kushman, Ph.D., M.P.H. previously worked as Toxicology Branch Chief (Detail, GS-14) at Fda and Supervisory Toxicologist (GS-14, Team Supervisor) at Fda. Mary Kushman, Ph.D., M.P.H. holds Master Of Public Health (Mph), Environmental Sciences And Engineering from University Of North Carolina At Chapel Hill.

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*@fda.gov
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AeroLeads found 1 current-domain work email signal for Mary Kushman, Ph.D., M.P.H.. Compare company email patterns before reaching out.

Profile bio

About Mary Kushman, Ph.D., M.P.H.

Experienced scientist with strong track record in toxicology, cancer biology, and public health. Specialized in scientific review of regulatory submission and evidence-based human health risk assessments of toxicological hazards. Skilled in developing and applying methods to synthesize large-scale information essential for decision-making processes within government regulatory agencies and businesses.

Listed skills include Cell Culture, Hplc, Spectroscopy, Enzyme Kinetics, and 14 others.

Current workplace

Mary Kushman, Ph.D., M.P.H.'s current company

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FDA
Fda
Toxicology Branch Chief
silver spring, maryland, united states
Website
Employees
14770
AeroLeads page
15 roles · 29 years

Mary Kushman, Ph.D., M.P.H. work experience

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

Toxicology Branch Chief

Current
Fda

Silver Spring, Maryland, United States

Nov 2023 - Present

Toxicology Branch Chief (Detail, Gs-14)

Fda
Sep 2022 - Nov 2023

Supervisory Toxicologist (Gs-14, Team Supervisor)

Fda

Calverton, Md

• Supervises a team of three to six toxicologists of varying experience levels in CTP's Office of Science, Division of Nonclinical Science, as their first managerial point-of-contact for work matters, including secondary/tertiary review of regulatory applications, distribution of workload, and performance evaluations.• Lead author on and contributor to key scientific memoranda for Division, leader of review teams for various regulatory submissions, and subject matter expert in areas of hazard assessment and systematic review.

Feb 2021 - Sep 2022

Supervisory Toxicologist (Gs-15, Branch Chief Detail)

Fda

Calverton, Md

• Directly supervised three supervisory team lead toxicologists, each of whom led a team of three to six toxicologists, pharmacologists, and biologists.• Communicated regularly with Division and Office leadership on matters related to scientific and professional activities/initiatives and involvement of branch personnel.• Led biweekly branch meetings, disseminating and discussing information pertaining to Center, Office, Division, and Branch activities.• Provided feedback on Division research priorities, scientific memoranda, regulatory submissions, and provided input as a subject matter expert when and where warranted.

May 2021 - Sep 2021

Lead Toxicologist (Gs-14)

Fda

Silver Spring, Maryland, United States

• Familiar with day-to-day schedules of reviewers, including regulatory review workload across several different submission pathways, workgroup participation, and research project participation.• Ensures even distribution of workload amongst team members.• Recommends team members for review of regulatory submissions and other division and center activities as appropriate for reviewer’s workload, interests, and experience level.• Serves as a mentor for and observes training needs of primary review staff, making recommendations to staff members and supervisors to encourage professional growth and ensure performance goals are met.• Provides routine feedback on performance.

Apr 2016 - Feb 2021

Toxicologist (Gs-13)

Fda

Silver Spring, Maryland, United States

• Performed primary, secondary, and tertiary toxicological review of regulatory submissions in the context of whether the products within raise different questions of public health• Developed systematic frameworks to synthesize and present scientific evidence for research questions relevant to CTP priorities.• Led a workgroup focusing on systematic review.• Co-authored peer-reviewed scientific papers on modes and mechanisms of action of tobacco toxicants and their relevance to smoking-related diseases.• Served as a point of contact for several research projects relevant to tobacco use, exposure, and toxicity for NIH- and CTP-funded grants.

Jan 2015 - Apr 2016

Toxicologist (Gs-12)

Fda

Silver Spring, Maryland, United States

See above description overviewing GS-13 duties.

Dec 2013 - Jan 2015

Orise Fellow

Development and implementation of systematic literature review frameworks and presentation of scientific evidence for health risk assessments, development of chemical hazard characterizations, and toxicological reviews. Special emphasis on evidence identification, selection, and presentation for chemical mode-of-action as related to carcinogenicity.Specific accomplishments include:*Development of criteria to determine the adequacy of toxicological and epidemiological studies.*Co-authored toxicological reviews of environmental and industrial chemicals as an integral part of multidisciplinary teams.*Performed major literature review, critical toxicity analysis and interpretation, and context of toxic and carcinogenic potential of phthalate esters, with particular emphasis on analysis of in vivo data for translation of toxicity to humans, conducted in collaboration with interdisciplinary teams of investigators.*Work selected for presentation at 2013 Society of Toxicology Annual Meeting.*Work featured in the UNC Gillings School of Global Public Health news for October 31, 2012, and in the Association of Schools of Public Health Friday Letter, November 9, 2012. Manuscript submitted to RegulatoryToxicology and Pharmacology.*Invited speaker at US EPA symposia, ICF International, and Integrated Risk Information System (IRIS) meetings.

Jun 2012 - Nov 2013

Scientific Communications Consultant

Integral Molecular

Philadelphia, Pa

Worked alongside junior and senior scientists assisting with technical writing, report presentation, and grant preparation in the areas of virology, immunology, and tropical medicine.

Oct 2011 - Dec 2011

Life Sciences And Intellectual Property Consultant

Penn Biotech Group

Advised Philadelphia-area contract research organizations and biotech startups on matters of protection of their intellectual property, proprietary assay development, and business development strategies.

Sep 2010 - Dec 2011

Technology Transfer Volunteer

Preparing summaries of technology from FCCC available for licensing and working to identify potential licensees for said technologies. Exposure to records of invention, drafted patent applications, and advised on proper handling of confidential material.

Nov 2010 - Sep 2011

Research Fellow

Designed and executed research problems relevant to carcinogen metabolism in human lung cell lines. Regularly presented research findings at international conferences and to laboratory group as part of routine in-house group meetings. Also responsible for aspects of laboratory management such as maintenance of cell culture facilities, carcinogen stocks, and chemical hygiene protocols.Three presentations at American Chemical Society or Society of Toxicology annual meetings, and appeared as a co-author publication in Chemical Research in Toxicology.Relevant skills: Radiometric reverse-phase high-pressure liquid chromatography, liquid scintillation counting, organic solvent extraction, real-time PCR, SDS-PAGE, Western blotting, protein purification, UV/visible spectroscopy, ethoxyresorufin-O-deethylase activity assay, aldo-keto reductase enzyme activity assays, and mammalian cell culture. Familiar with liquid chromatography/mass spectrometry.

Sep 2007 - Dec 2010

Research Fellow

Vanderbilt University Medical Center

Proposed research problems relevant to DNA polymerase bypass of bulky nucleic acid adducts. Research findings and proposals regularly discussed in front of laboratory group and departmental research specialty section.Relevant skills:Fast-pressure liquid chromatography, SDS-PAGE, Western blotting, and growth of bacterial cell cultures. Familiar with Matrix-assisted Laser Desorption/Ionization-Time of Flight Mass Spectrometry (MALDI-TOF).

2005 - 2007 ~2 yrs

Cancer Biology Doctoral Student

Wake Forest University School Of Medicine

Investigated protective mechanisms against the toxicological action of polycyclic aromatic hydrocarbons in cells engineered to express specific human cytochrome P450 and glutathione-S-transferase isoforms.Eight presentations at American Association for Cancer Research annual meetings or International Society for the Study of Xenobiotics meeting, and published in Carcinogenesis, Mutation Research, and Toxicological Sciences.

2000 - 2005 ~5 yrs

Master'S Candidate, Molecular Biology And Biotechnology

East Carolina University

Designed and performed studies investigating bioenergetics of normal versus cancerous breast epithelial cells.

1998 - 2000 ~2 yrs
Team & coworkers

Colleagues at FDA

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5 education records

Mary Kushman, Ph.D., M.P.H. education

Ms, Molecular Biology And Biotechnology

Activities and Societies: Beta Beta Beta Biological Honor Society President, 1998-1999.Relevant skills: Mammalian cell culture, Western.

Bs (Cum Laude), Physics (Biophysics)

Activities and Societies: Sigma Pi Sigma Physics Honor Society (Secretary), Sarah Patterson Lane Award for Undergraduate Achievement.

Education record

Hunt High School

Top 2% of graduating high school class. Active in science and math activities with multiple Science Olympiad awards. Served as an officer.

FAQ

Frequently asked questions about Mary Kushman, Ph.D., M.P.H.

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

What company does Mary Kushman, Ph.D., M.P.H. work for?

Mary Kushman, Ph.D., M.P.H. works for FDA.

What is Mary Kushman, Ph.D., M.P.H.'s role at FDA?

Mary Kushman, Ph.D., M.P.H. is listed as Toxicology Branch Chief at FDA.

What is Mary Kushman, Ph.D., M.P.H.'s email address?

AeroLeads has found 1 work email signal at @fda.gov for Mary Kushman, Ph.D., M.P.H. at FDA.

Where is Mary Kushman, Ph.D., M.P.H. based?

Mary Kushman, Ph.D., M.P.H. is based in Rockville, Maryland, United States while working with FDA.

What companies has Mary Kushman, Ph.D., M.P.H. worked for?

Mary Kushman, Ph.D., M.P.H. has worked for Fda, Us Epa, Integral Molecular, Penn Biotech Group, and Fox Chase Cancer Center.

Who are Mary Kushman, Ph.D., M.P.H.'s colleagues at FDA?

Mary Kushman, Ph.D., M.P.H.'s colleagues at FDA include Suraj Rajasimhan., Pharm.D., Bcps, Bcccp, Sungjoon "Alvin" Chi, Jinglin Zhang, Valerie D Davidson, and Nicole Gormley.

How can I contact Mary Kushman, Ph.D., M.P.H.?

You can use AeroLeads to view verified contact signals for Mary Kushman, Ph.D., M.P.H. at FDA, including work email, phone, and LinkedIn data when available.

What schools did Mary Kushman, Ph.D., M.P.H. attend?

Mary Kushman, Ph.D., M.P.H. holds Master Of Public Health (Mph), Environmental Sciences And Engineering from University Of North Carolina At Chapel Hill.

What skills is Mary Kushman, Ph.D., M.P.H. known for?

Mary Kushman, Ph.D., M.P.H. is listed with skills including Cell Culture, Hplc, Spectroscopy, Enzyme Kinetics, Molecular Biology, Western Blotting, Tissue Culture, and Cancer.

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