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Christina Ferguson
Clinical Research Data Manager, Georgetown University

Location: Washington DC, WA United States
Joined: Nov 16th, 2021
About   (request update)
Education   (request update)
Hampton University class of 2006
Undergrad Major: Psychology
Walden Univ class of 0
Grad Major: Psychology
Experience
I currently work with Georgetown University as Clinical Research Data Manager
I have years of experience working in the Research & Development industry.
Clinical Research Data Manager | ASRC Federal
From April 2022 to Current • 4 year(s)
Manages data for clinical trials phase I/II trials, maintains electronic databases, and coordinates with research teams for monitoring visits and audits.
Clinical Research Data Manager | Georgetown University
From January 2019 to May 2022 • 3 year(s)
Managed data for clinical trials of varying complexity, maintained electronic databases, and ensured compliance with regulatory requirements.
Site Coordinator | Advanced Clinical
From September 2017 to January 2018 • 1 year(s)
Managed administrative and clinical processes for Children's National Department of Neurology, maintained regulatory requirements and served as liaison between stakeholders.
Administrative Assistant | Medstar Georgetown University Hospital
From September 2015 to August 2017 • 2 year(s)
Provided administrative support to physicians, managed patient scheduling and registration, and prepared meeting agendas and minutes.
Lead Project Coordinator | American University
From January 2013 to September 2015 • 2 year(s)
Monitored and analyzed survey data, collaborated with school principals to conduct surveys, and oversaw research project execution to meet milestones.
Clinical Research Assistant | Children's National Medical Center
From July 2007 to March 2013 • 6 year(s)
Maintained participant research charts, assisted with patient eligibility screening, performed data extraction, and coordinated tumor board meetings.
Clinical Research Coordinator | Children's National Medical Center
From July 2007 to March 2013 • 6 year(s)
Worked with IRB and regulatory staff, maintained study documents, coordinated participant appointments, and ensured adherence to clinical trial protocols.
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