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Q&A With Donna Pryor

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Donna Pryor
Sr. Clinical Research Associate, Merck
Location: Upper Marlboro, MD United States
Joined: Nov 30th, 2021
About   (request update)
Education   (request update)
Howard University class of 2004
Undergrad Major: Genetics
Experience
I currently work with Merck as Sr. Clinical Research Associate
I have years of experience working in the Biotechnology and Pharmaceutical industry.
Sr. Clinical Research Associate | Merck
From August 2019 to Current • 7 year(s)
 Senior clinical research associate responsible for clinical monitoring and trial oversight.
Senior Clinical Research Associate | PRA Health Sciences
From October 2014 to August 2019 • 5 year(s)
 Independently performed clinical monitoring processes, provided site management and training, and ensured regulatory compliance for investigational products.
Lead Clinical Research Associate/Acting Clinical Project Manager | PharmAthene
From November 2013 to July 2014 • 1 year(s)
 Functioned as Clinical Project Manager, provided clinical oversight of CRO, and managed vendor and site selection for clinical trials.
Sr. Clinical Monitoring Associate | PAREXEL
From September 2012 to November 2013 • 1 year(s)
 Performed remote clinical monitoring tasks, negotiated site contracts, and trained study sites on protocols and policies.
Senior Regional Clinical Research Associate | RPS
From May 2010 to August 2012 • 2 year(s)
 Analyzed clinical data, conducted monitoring visits, managed trial master files, and provided training to CRAs and site personnel.
Senior Clinical Research Associate | PPD
From July 2005 to April 2010 • 5 year(s)
 Coordinated clinical monitoring processes, conducted site visits for compliance, and developed relationships with investigative sites and pharmaceutical officials.
Study Coordinator | Howard University Hospital
From July 2003 to July 2005 • 2 year(s)
 Coordinated HIV and sickle cell disease clinical trials, recruited patients, and created educational materials for community outreach.
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