Featured Member: Brittany Duke on HBCU CONNECT!

Connect with Brittany

• Email Me or Poke Me
• Interview Me
• Send Group Invite
• Add To Favorites
• Block This Member
• Send Friend Request

Uploads

Upload Content | Show More

Connections

more-->

Recent Visitors

more-->

More Members

more-->

Q&A With Brittany Duke

(interview me)

Brittany Duke
UM Pharmacist , Examworks UM Strategies
Location: Lanham , MD United States
Joined: Mar 16th, 2026

About (request update)

Education (request update)

University of Maryland at Col Park class of 2008

Undergrad Major: Microbiology

University of Maryland Eastern Shore class of 2014

Grad Major: Pharmacy

Experience

I currently work with Examworks UM Strategies as UM Pharmacist
I have 18 years of experience working in the Biotechnology and Pharmaceutical industry.

Utilization Management Pharmacist | Examworks UM Strategies
From November 2025 to Current • 1 year(s)
Writes comprehensive evidence-based Rx Analysis reports and supports pharmacist staff in performing outreaches to medical providers.

Pharmacist | FDA
From July 2024 to May 2025 • 1 year(s)
Provided pharmacist expertise in the Office of Generic Drugs, evaluating ANDAs and supporting generic drug approval processes.

Founder & Owner/Health Content Strategist | Rx Care Consulting LLC
From May 2020 to July 2024 • 4 year(s)
Provided pharmacist expertise as medical reviewer and created health content marketing services for pharmacy consulting companies.

Associate Director, Regulatory Affairs (Global Biosimilar) | Fresenius Kabi USA LLC
From June 2022 to May 2024 • 2 year(s)
Provided global regulatory leadership for biosimilar development and managed submission strategies and health authority interactions.

Senior Manager Clinical Regulatory Affairs | Pardes Biosciences Inc.
From March 2022 to June 2022 • 0 year(s)
Served as global regulatory lead for PBI-0451 antiviral drug development and prepared regulatory documents for clinical trial authorizations.

Global Regulatory Manager | Bristol Myers Squibb
From May 2021 to March 2022 • 1 year(s)
Managed global regulatory affairs operations for Nivolumab Lung Cancer Portfolio and supported health authority interactions.

Subject Matter Expert III- Medical Writer/Analyst IV | Brillient Corporation
From June 2020 to May 2021 • 1 year(s)
Developed regulatory documents and conducted data analysis for FDA's Division of Medication Error Prevention and Analysis.

Drug Safety Specialist/Operations Specialist III | IQVIA
From March 2021 to April 2021 • 0 year(s)
Created adverse event reports and processed safety data for the Moderna COVID-19 vaccine.

Pharmacist II- Medical Writer- Project Manager | Chenega Professional and Technical Services
From August 2019 to May 2020 • 1 year(s)
Performed post-market drug surveillance data analysis and developed work instructions for FDA import compliance.

ORISE Post-Doctoral Fellow- Medical Writer- Project Manager | FDA
From July 2017 to August 2019 • 2 year(s)
Worked on systemic biologics research projects and analyzed geriatric drug labeling for regulatory compliance.

ORISE Post-Doctoral Fellow- Medical Writer- Project Manager | FDA
From August 2017 to October 2018 • 1 year(s)
Managed special project on anti-psychotic drug-induced severe cutaneous adverse reactions and conducted FAERS data analysis.

Remote Pharmacogenomics Certification Pharmacist | RxIGHT
From August 2016 to June 2017 • 1 year(s)
Performed personalized medication reviews with patients and trained other pharmacists for certification programs.

ORISE Health Care Quality Fellow- Medical Writer- Project Manager | US Department of Health and Human Services
From February 2016 to August 2016 • 0 year(s)
Worked with National Action Plan for Adverse Drug Event Prevention and created presentations on pharmacist roles in patient safety.

Clinical Staff Pharmacist | Holy Cross Hospital
From December 2014 to February 2016 • 2 year(s)
Supervised IV room workflow, verified physician orders, and provided clinical knowledge to healthcare providers in various units.

Clinical Research Associate | Renaissance RX
From September 2014 to December 2014 • 0 year(s)
Performed clinical trial data analysis and provided pharmacogenomics consultation for the Diagnosing Adverse Reactions Trial.

My Groups

Invite Me To A Group

Guestbook Comments