Bridget Nwaogu

713-***-**** adg38q@r.postjobfree.com

** ***** ** ********** ****** the medical field,. I can work independently or as a team player. I am a reliable, self-motivated and driven to create high and efficient work quality . I provide safe, supportive, and individualized care for all my patients. I have strong communication, interpersonal, organizational, time management, analytical and problem solving skills. I have the ability to learn and apply new procedures quickly; organize and prioritize tasks to meet deadlines and adapt readily to new challenges.

WORK EXPERIENCE

Nurse Practitioner

October 2019-current Texas Liver Institute, Sub-Investigator/Manager Houston, TX

Supporting the principle investigator and oversee the execution of study protocols, delegating study related duties to site staff, as appropriate, and ensuring site compliance with study protocols, study-specific laboratory procedures, standards of Good Clinical Practice (GCP), Standard Operating Procedures (SOPs), quality (QA/QC) procedures, OSHA guidelines, and other state and local regulations as applicable.

Provides medical management, screen, and recruit Hepatology patients for phase 1-4

Obtain informed consent, enrolled and maintained study subjects

Confirm eligibility of study subjects, also collected, recorded completed case report form, completed subject study binders, reporting AE/SAEs in a timely manner, entering data into several Sponsor’s databases.

Reviewing labs and test results, reporting any clinical significant or abnormalities findings to the PI for further direction.

Sign prescriptions and perform clinical examinations,

evaluated laboratory and other medical reports.

Supervise administration of study drug

Maintain accurate accountability for all clinical supplies received by site

Observe, measure and record effects of drug

Evaluate, manage and report all adverse events, analyzed clinical research data to ensure accuracy, quality and consistency between source documents as well as proper, timely reporting of critical study events.

Keep and make study documentation available for data verification purposes

GCP and HIPAA trained, SIVs, interaction and submission to the IRB, study closeouts.

Performed blood draws, specimen shipments, ECGs, vital signs, and managing IP.

Represent as the company Sub-Investigator at Investigator Meetings around the US

September 2017-September 2019 Low-T Center 2nd Clinical Provider, Friendswood, TX

Second Provider responsible for assisting the Center Director, including but not limited to, overseeing the daily lab operations, providing treatment to the patients and establishing a positive relationship

Direct patient interaction, within men’s clinic to manage hypogonadism, obstructive sleep apnea, hypothyroidism, chronic allergies, hypertension, diabetes and high cholesterol

treat patient through defined, established, and peer-reviewed protocol; along with full evaluation of the root cause of these conditions.

monitoring the lab for accurate calibrations and controls.

Determines abnormal conditions by administering or ordering diagnostic tests, MRIs, electrocardiograms, and laboratory studies; interpreting test results.

Registered Nurse

August 2013-September 2017 Houston Methodist CVIMU/ PRN, Houston, TX

Provide direct patient care effectively and efficiently to the patient which may include patients with varied and complex needs.

assumes leadership roles with progressive responsibility including but not limited to participating in or leading unit and shared governance initiatives, serving as a preceptor to students or new employees

possibly contributing to service line or hospital wide

Houston Methodist Research, Houston, TX

Provide care to all study subjects within the standards set forth by facility.

Safely and effectively administer study medications. Accurately document the administration of study medication in the source document and MAR sheet (for inpatient). Captures pertinent data onto source documents (i.e., vital signs, adverse events, concomitant medications, etc.). Reports and documents serious adverse events on a timely manner.

Responsible for gathering necessary information from the research participants (i.e. HIPAA, Medical Chart Release Authorization, Questionnaires).

Responsible for the Informed Consent Process per the SOPs. Responsible for reviewing inclusion and exclusion criteria for the PI. Responsible for completing all study specific procedures according to the study protocol. Review subject’s information in preparation for the investigator’s review.

Ensure the diagnostic specimens are packaged per IATA guidelines

Screens all inpatients daily for all open studies and enrolls patients according to specific protocol requirements. Completes medical trials electronic daily screening/enrollment log on a daily basis.

June 11-April 2012 Department of Aging &Disability Services Brenham, TX

Performs health assessments; Discharge Planning, Nursing Assessment and Care Screening. Administers medication/treatments safely

Coordinates clinics, schedules individuals in appropriate clinics, assures clinics are staffed appropriately, informs physician of changes in individual, and communicates accordingly

EDUCATION

Masters in Nursing, University of Texas Health Science Center

(December 2016)

Bachelors of Nursing, Texas Tech University Health Science Center (December 2011)

Associate Degree in Nursing, San Jacinto Community College, Pasadena, TX (December 2010)

LICENCES / CERTIFICATION

AANP certification F03170601

APRN license AP133923

DEA

RN license 797520

Certified CPR/BLS/ACLS

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