Data Entry Assistant Clinical
Resume:
Ednita Gonzalez-Jasso
Pasadena, Tx
***********@*****.***
Experience
Clinical Research
HD Research, Bellaire, TX
To become familiar with ongoing protocols, Pre-screen potential subjects, consent and
perform screening, follow up visits and, post-surgical floor assessments. As a lead
Coordinator, communicate with study Monitors and sponsors, develop study source, track
study visits, update study staff of protocol changes including new source or ICF.
Communicate with referring physicians for recruiting.
Feb 2021- Present
Mobile Phlebotomist Team Lead Apheresis Tech 1
Gulf Coast Reginal Blood Center, Houston, TX
To unload and load mobile equipment, set up and supervise
mobile drive. Perform all quality control test, ensure staff is
following protocol. Delegate work, oversee the blood drive,
address any custom complaints or concerns during the blood,
conduct pre-donation physical, screening and questionnaire,
perform phlebotomy for whole blood and apheresis donations.
Clinical Research Coordinator
AMCR Institute, Inc., Escondido, Ca
Perform data entry into eCRF, create source documents according to sponsor protocol,
perform vital signs, collect and process lab samples,
assess subject compliance to study protocol, device accountability, perform ECG, insertion of CGM and insulin infusion sets. IATA certified.
Assistant Clinical Research Coordinator
Institute of Health Care Assessment, San Diego, Ca
Informed Consent, Maintain Patient Records, Patient
Screening, Patient Enrollment, Appointment Scheduling, Perform Scheduled Visit Tasks, Spirometry Testing/Readings, ECG testing/transmission, Phlebotomy &Lab Processing,
assist coordinator and physician with procedures and physicals.
May 2015
-Feb2021
Aug2011
-Aug2012
Oct-2009
-Feb2011
Clinical Research Associate
Veterans Medical Research Foundation, San Diego, CA
2008 – 2009
Manages and oversees protocols and is responsible for the protocol review and
approval process to regulatory agencies. Assists with the
implementation of study-specific procedures, methods, guidelines, and tools.
Responsible for identifying and reporting any problems and/or issues in order to
ensure that all clinical aspects of studies are being carried out in accordance with state and federal regulations, guidelines and policies. Manages all on-site files and records, case report forms, and source documents for accuracy, consistency, and compliance.
Interviews potential study candidates and makes the initial decision for further evaluation. Collecting and processing central and local labs, entering study visits to EDC
portals.
Laboratory Technician I
Veterans Medical Research Foundation, San Diego, CA
2006 – 2008
Phlebotomist III
VA San Diego Healthcare System, San Diego, CA
2005 – 2010
Certification & Training
Citi Training
GCP
IATA
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