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Research Associate Coordinator

Location:
Houston, TX
Salary:
80k annual
Posted:
March 25, 2023

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Resume:

Curriculum Vitae

Name Zainab Agboola Mcghie

Address ***** *******, *****.

Phone number 713-***-****

Email *******************@*****.***

Experienced Clinical Research Associate functions in monitoring various phases of clinical trials of drugs. Clinical Research Associate

Dyne Therapeutics, San Antonio, Texas.

Oncology, Medicine and Obstetrics & Gynecology

Sites Monitoring from IMV through COV

Prepares Laboratory, processing volunteers, taking biological samples or vital signs and organizing data

Assist research nurses with progress reports for industry sponsored clinical trials Record readings in Excel while CRA reviews slides

Coordinate pickup/transport of research Investigative Product Screen, consent and enroll patients in ED research studies Assist with subject assessments during study participation Updates documents on ICF, ISF, EDC, VEEVA VAULT, EXCEL POWERPOINT e.t.c. Sep 2021 - Feb 2023

Clinical Research Coordinator

Ventavia Research Group, Houston, Texas

Assists Principal Investigator to assure that all key personnel or persons engaged in the research project have met training requirements in accordance with Federal Regulations. Prepares study materials which include but not limited to ICF, CRFs, Enrollment Logs and drug/device accountability logs as requested by the PI.

Attends investigator means required or requested by the PI. Registers participants to the appropriate coordinating center ( in case of multi site study ) Retains all study records, completes study documentation and maintains study files in accordance with sponsor requirements, policies and procedures. Reviews and accepts/corrects the billing of study procedures to the appropriate research fund, Develops and maintains study specific documentation and Data Management guidelines. Takes appropriate steps to avoid conflicts of interest or the appearance of conflicts of interest and reports instances of noncompliance to the appropriate compliance office. Collects documents needed to initiate the study for submission to the sponsor ( e.g., FDA Forms 1572, CVs, e.t.c. )

Works with Environmental Health and Safety to ensure that all facilities used are in compliance with all applicable regulations.

Maintains copies of any applicable facility audits and equipment inspection/service reports. Screens subjects for eligibility using protocol specific inclusion and exclusion criteria. Jun 2019 - Jul 2021

PERSONAL

RESUME OBJECTIVE

WORK EXPERIENCE

EDUCATION AND QUALIFICATIONS

Bachelor of Science

University of Ilorin, Nigeria

Sep 2007 - Mar 2012

Practical Nursing ( In Review )

Sacred Heart School of Nursing, Houston, Texas

Nov 2020 - Nov 2023

High proficiency with

full Microsoft app.

Time Management

Problem-Solving

skills

Conflict Management

Customer Service

Experience

Research

Organizational skills

Communication

SKILLS



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