Summary
Overview
Work History
Education
Skills
Certification
Work Availability
Quote
Timeline
Additional Information
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UCHE BRIGHT

UCHE BRIGHT

Clinical Research Associate
Dallas,TX

Summary

Detail-oriented Clinical Research Associate with experience in conducting phases I-III Clinical trials. Proficient in leading various site visits, including PSSV, SIV, IMV, COV, etc. Specializes in therapeutic areas such as Medical devices, Oncology, CNS, Endocrinology (particularly diabetes), Rare diseases, and pain management. Demonstrates a quick grasp of new procedures and possesses advanced planning, problem-solving, and communication skills honed over 7+ years of successful clinical research experience.

Overview

1
1
Certification
6
6
years of professional experience
7
7
years of post-secondary education

Work History

Senior Clinical Research Associate

ERGOMED
Atlanta , GA
08.2019 - 07.2021
  • Conducted phases I, II & III clinical trials in oncology (ovarian, breast, renal cell carcinoma, and advanced solid tumors) in adult subjects
  • Worked on first-in-human, dose escalation and dose expansion studies with RECIST 1.1 evaluations
  • Served as the main point of contact for clinical sites and ensured compliance with protocol, GCP and regulatory requirements
  • Performed 100% SDV and risk-based monitoring using the AIM method during on-site and/or remote visits using electronic EDC and in-house local CIMS system
  • Maintained regular site staff contacts, training and query resolution support
  • Participated in local interim analysis

Clinical Research Associate

ICON
New York, NY
02.2015 - 08.2019
  • Conducted phases I-III clinical trials in various therapeutic areas such as mental disorders, infectious diseases, respiratory diseases, medical devices, hematology/oncology, genitourinary diseases and rare/genetic diseases
  • Performed start-up activities, initiation, interim and close-out monitoring visits
  • Performed 100% SD and risk-based monitoring using the AIM method during on-site and/or remote visits using electronic EDC and in-house local CTMS system
  • Reviewed diaries and on-site investigator files and ensured subject safety by overseeing timely and accurate AE/SAE reporting and follow-up
  • Used IT and IVRS for IP set-up, accountability and management
  • Maintained regular site staff contacts, training and query resolution support
  • Participated in local interim analysis

Education

M.D. - Medicine

Ahmadu Bello University
Zaria, Nigeria.
02.2008 - 11.2014

Skills

  • Research Experience
  • Experienced in Microsoft office products ( Word, Excel, PowerPoint, SharePoint, Teams etc)
  • Proficient in the use of Clinical trial systems like, EDC, CTMS, eTMF,
  • Excellent Organizational skills
  • Excellent Communication skills both verbal and writing skills
  • Multitasking
  • Strong interpersonal skills
  • Leadership skills
  • Proficient in ICH/GCP and FDA CFR requirements and other international regulations and directives
  • Medical Terminology
  • Team player
  • Good documentation practice following ALCOA-C principles

Certification

  • ICH/GCP Certified
  • BLS
  • Medical and Dental council Of Nigeria.

Work Availability

monday
tuesday
wednesday
thursday
friday
saturday
sunday
morning
afternoon
evening
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Quote

How many ideas have there been in the history of the human race that were unthinkable ten years before they appeared?
Fyodor Dostoevsky

Timeline

Senior Clinical Research Associate

ERGOMED
08.2019 - 07.2021

Clinical Research Associate

ICON
02.2015 - 08.2019

M.D. - Medicine

Ahmadu Bello University
02.2008 - 11.2014

Additional Information

PUBLICATION

Journal Of Medicine In The Tropics ( year 2019, volume 21, issue 2, pages 73-80)- Knowledge, attitude. and practice of hand washing among healthcare workers in a tertiary health facility in northwest Nigeria

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UCHE BRIGHT Clinical Research Associate