Featured Member: Aleina Surratt on HBCU CONNECT!

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Aleina Surratt
Senior Clinical Research Associate, International Clinical Research Partners
Location: Washington, DC United States
Joined: Jul 7th, 2007

About (request update)

Education (request update)

University of Denver class of 2000

Undergrad Major: Biology

Experience

I currently work with International Clinical Research Partners as Senior Clinical Research Associate
I have years of experience working in the Science industry.

Senior Clinical Research Associate | International Clinical Research Partners
From December 2016 to Current • 10 year(s)
Monitor clinical studies according to SOPs and FDA/GCP/ICH guidelines while ensuring patient safety and maintaining data integrity. Conduct qualification, interim, routine, and closeout site monitoring visits for various therapeutic areas.

Senior Clinical Research Associate | Chiltern International
From January 2016 to December 2016 • 0 year(s)
Monitored clinical studies according to SOPs and FDA/GCP/ICH guidelines while ensuring patient safety and maintaining data integrity. Managed site monitoring for 15 clinical research centers for Ophthalmology studies.

Senior Clinical Research Associate (Site Manager) | Novartis/GSK Vaccines
From July 2014 to December 2016 • 2 year(s)
Monitored clinical studies for infectious disease trials including influenza, Group B Streptococcus, and meningitis studies. Conducted study feasibility, site selection, and managed communication between sponsors and research units.

Senior Clinical Research Associate | Parexel International
From August 2011 to April 2014 • 3 year(s)
Managed site monitoring for 30 clinical research centers for dual arthritis studies across multiple countries. Responsible for issue resolution, patient enrollment, and ensuring timely quality data entry at sites.

Clinical Project Coordinator | Emmes Corporation
From May 2009 to August 2011 • 2 year(s)
Managed two clinical research units with over 50 food and waterborne disease clinical research projects for Tufts University and Washington State. Coordinated communication between sponsors and research units.

Clinical Research Monitor | Emmes Corporation
From May 2008 to August 2011 • 3 year(s)
Monitored ophthalmology clinical research trials at the National Eye Institute including age-related macular degeneration and diabetic retinopathy studies. Conducted protocol compliance monitoring, safety assessments, and pharmacy audits.

Quality Assurance Auditor/Specialist III | United Therapeutics
From February 2006 to May 2008 • 2 year(s)
Managed and conducted internal, site and vendor audits to ensure study protocol and regulatory compliance for an Ovarian Cancer clinical trial. Reviewed and approved SOPs, batch records, protocols, and validation reports.

Quality Control/Analyst | Fisher Clinical Service
From September 2001 to February 2005 • 4 year(s)
Implemented cGMP compliance practices and wrote Quality Control/Assurance SOPs. Monitored batch record productions and performed cGMP/GLP audit inspections to ensure FDA regulations.

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