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Christopher Duncan Email & Phone Number

MPH, PMP, Program Management Analyst at FDA
Location: Silver Spring, Maryland, United States 7 work roles 3 schools
1 work email found @fda.gov LinkedIn matched
✓ Verified July 2026 4 data sources Profile completeness 100%

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Current company
FDA
Role
MPH, PMP, Program Management Analyst
Location
Silver Spring, Maryland, United States
Company size

Who is Christopher Duncan? Overview

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Quick answer

Christopher Duncan is listed as MPH, PMP, Program Management Analyst at FDA, a with 14770 employees, based in Silver Spring, Maryland, United States. AeroLeads shows a work email signal at fda.gov and a matched LinkedIn profile for Christopher Duncan.

Christopher Duncan previously worked as Program Management Officer at Fda and Regulatory Research Project Manager at Fda. Christopher Duncan holds Master Of Public Health (Mph), Health/Health Care Administration/Management from Loma Linda University.

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{first}.{last}@fda.gov
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Profile bio

About Christopher Duncan

Directs regulatory research projects and activities. Facilitates acquisition planning, statement of work (SOW) development, and assures stakeholder engagement. Manages all actions for assigned major contracts to include development of procurement requirements, pre-award, and post-award activities as a Contracting Officer's Representative (COR) Level III.

Listed skills include Project Management, Government, Microsoft Excel, Contract Management, and 1 others.

Current workplace

Christopher Duncan's current company

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FDA
Fda
MPH, PMP, Program Management Analyst
silver spring, maryland, united states
Website
Employees
14770
AeroLeads page
7 roles

Christopher Duncan work experience

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Program Management Officer

Current
Fda

Silver Spring, Maryland, United States

Provides technical assistance for all phases of contracts within Offices/Divisions. Uses own judgment to independently write or rewrite performance work statements for solicitations, re-solicitations, and follow-on contracts. Independently designs and performs contract quality assurance for each requirement. Exercises management oversight of obligation of expenditure of funds and establishes internal controls to prevent fraud, waste, and abuse. Finalizes changes to contracts for content, format, and acceptability. Advises management and staff on all contract current and proposed policies. Recommends changes to existing policies and procedures. Determines whether contractor performed work meets standards of adequacy before authorizing payment. Finalizes contracts and solicitations to ensure appropriate quality control requirements are imposed prior to submission to FDA, Office of Acquisitions and Grants Services (OAGS).

Aug 2023 - Present

Regulatory Research Project Manager

Current
Fda

Silver Spring, Md

Coordinates regulatory science research projects and activities.Participates in acquisition planning, statement of work (SOW) development, team meetings, and assures stakeholder engagement as appropriate.Contracting Officer's Representative (COR) FAC-COR Level III. Manages all actions for major contracts to include development of procurement requirements, pre-award and post award requirements to oversight and contract close-out.

Oct 2017 - Present

Management And Program Analyst

Fda

Silver Spring, Md

Manages assigned contracts within the Office of Pharmaceutical Quality as the lead Contracting Officer’s Representative (COR).Executes a variety of actions supporting FDA’s national commitment to science education as liaison for the office’s Oak Ridge Institute for Science and Education (ORISE) Fellowship Training Program.

Feb 2015 - Oct 2017

Program Coordinator

Fda

Silver Spring, Md

Coordination activities oversee administration, facilities, procurement, and operations while directly assisting the Director and Deputy Director in the financial management of key research programs.Directs the actions of the division's Safety Team, Equipment Maintenance Team, and the Facilities Infrastructure Team.

Mar 2013 - Feb 2015

Scientific Reviewer

Fda

Silver Spring, Md

Evaluate scientific data in the area of hematology in vitro diagnostic medical devices and submits reports on a variety of regulatory actions. Interactively reviews, provides direction and guidance to medical device manufacturers regarding the scientific data used to evaluate in vitro diagnostic device 510(k) submissions.

Mar 2010 - Feb 2013

Chief Technologist

Whiteriver, Az

Supervise the Hematology Department located within the clinical laboratory.Assure that blood specimens submitted for testing in the Hematology Department meet laboratory guidelines.Train personnel in the use of laboratory equipment.Oversee whole blood glucose monitoring system for hospital staff of 383 employees, generating 18,178 results annually.Detect and resolve discrepancies in patient results.Maintain special chemistry instruments located in the clinical laboratory.Produce accurate and timely results according to laboratory policy.Collect quantities of blood by venipuncture and capillary methods as appropriate for patient age and/or condition.Perform and record quality control function checks with the specified time frame.

Mar 1998 - 2010

Staff Technologist

Parker, Az

Perform and document preventative maintenance on laboratory instrumentation.Detect and resolve discrepancies in patient results.Produce accurate and timely results according to laboratory policy.Insured that all Material Safety Data Sheets (MSDS) were current in laboratory and notified staff of any harmful chemicals contained in testing reagents.Organized continuous quality improvement effort for Colorado River Service Unit and was team leader for this committee.

Jan 1995 - Mar 1998
Team & coworkers

Colleagues at FDA

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3 education records

Christopher Duncan education

Bachelor Of Science In Health Sciences, Clinical Laboratory Science/Medical Technology/Technologist

Post Baccalaureate Certificate, Project, Program & Portfolio Management

FAQ

Frequently asked questions about Christopher Duncan

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What company does Christopher Duncan work for?

Christopher Duncan works for FDA.

What is Christopher Duncan's role at FDA?

Christopher Duncan is listed as MPH, PMP, Program Management Analyst at FDA.

What is Christopher Duncan's email address?

AeroLeads has found 1 work email signal at @fda.gov for Christopher Duncan at FDA.

Where is Christopher Duncan based?

Christopher Duncan is based in Silver Spring, Maryland, United States while working with FDA.

What companies has Christopher Duncan worked for?

Christopher Duncan has worked for Fda and Indian Health Service.

Who are Christopher Duncan's colleagues at FDA?

Christopher Duncan's colleagues at FDA include Daphne Stewart, Tara Herrmann, Wiley Carr, Carletta Moore, and Dharam Padhaya Pmp, Msit/Mis, Mba, Ph.D.

How can I contact Christopher Duncan?

You can use AeroLeads to view verified contact signals for Christopher Duncan at FDA, including work email, phone, and LinkedIn data when available.

What schools did Christopher Duncan attend?

Christopher Duncan holds Master Of Public Health (Mph), Health/Health Care Administration/Management from Loma Linda University.

What skills is Christopher Duncan known for?

Christopher Duncan is listed with skills including Project Management, Government, Microsoft Excel, Contract Management, and Ms Project.

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