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Clinical Research Assistant

Location:
Saint Paul, Minnesota, United States
Posted:
December 19, 2018

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Resume:

RESUME

Gonzalo Suarez MD, PHD

**** ******** *****, *****, **, 55122

Phone : 612-***-****

Email: ac70io@r.postjobfree.com

Objectives: To contribute to the Clinical Research field where I will be able to help the whole team comply with all the recruitment process, required regulations, Case Report Forms, Reporting Adverse Events, serve as a Liaison between IRB and the Trial site and prevent unnecessary delays in the initiation and guaranteed the timely completion of clinical trials also prevents any protocol deviation and reassure FDA regulatory compliance.

Summary of qualifications:

Expertise on Medical Terminology.

Vast experience in Management of Clinical Devices Complaints.

Extensive training experience, supervising personnel and coordinating activities among members of healthcare teams.

Knowledgeable administering Informed Consent and carrying out the recruitment of subjects.

Planned safety strategy for the prevention of adverse effects during studies and designing protocols for reporting adverse events to the IRB’s.

Detection and reporting adverse events of experimental protocols to participants, Principal Investigators, primary care physicians and IRB.

Collected data on medications and evaluated their effects on experimental protocols.

Good capacity to manage, follow standard operating procedures and execute research projects to full completion and complete understanding of good clinical practices

Respectful and compliant with IRB protocols, HIPAA guidelines and FDA regulations.

Knowledgeable in the use of all Microsoft office programs and extensive knowledge of In Core, EPIC programs and EMR ( electronics Medical Records).

Detail and in depth knowledge of human physiology especially in the OBGYN field.

Fluent in English and Spanish.

Professional Highlights

4 articles published in peer reviewed journals

1 book chapter regarding puerperium infections

Contributing to one Clinical Trial “ Use of Entresto Sacubitril/Valsartan for the treatment of Peripheral Arterial Disease”, NCT02636283, at Minnesota University, under the supervision of Dr. Otto Sanchez.

Employment:

Clínica El Avila, Caracas, Venezuela, OBGYN Dept, January 1992 to October 2017.

Worked as a Clinical Research Assistant contributing to one Clinical Trial “ Use of Entresto Sacubitril/Valsartan for the treatment of Peripheral Arterial Disease”, NCT02636283, at Minnesota University, under the supervision of Dr. Otto Sanchez since February 2018 to October 2018.

Education :

Ph.D in Obstetrics and Gynecology, Universidad Central de Venezuela, Caracas, Venezuela,1986- 1989

M.D, Universidad Central de Venezuela, Caracas, Venezuela, 1978-1984

Certification :

Clinical Research Coordinator training certificate at Northwestern University Clinical and Translational Science Institute (NUCATS, Chicago, Il).

Collaborative Institutional Training Inicative ( CITI ) Good Clinical Practice course, approved.

American Board of Surgical Assistants ( ABSA), First Surgical Assistant Certified, Wisconsin, US,2017

Nuchal Translucency Determination, Fetal Medicine Foundation, Caracas Venezuela (2007)

First Trimester Screening for Aneuploidy, Reina Sofia Clinic, Bogota, Colombia ( 2007)



Contact this candidate