Ednita Gonzalez-Jasso

619-***-****

Pasadena, Tx

ads5gy@r.postjobfree.com

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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