GCP-certified Clinical Research Coordinator with over 5 years in healthcare and 3+ years executing clinical trials across Phases I–III in various therapeutic areas including Oncology and Immunology. Expertise in managing complex protocols, subject enrollment, and retention, along with remote and on-site source data verification. Proficient in ICH-GCP and FDA compliance, with extensive experience in eTMF systems and EDC platforms. Strong skills in regulatory document management and site readiness for audits and inspections.
Hi, I’m
CHIDERA EZIRI
Charlotte,NC
Summary
Overview
5
years of professional experience
1
Certification
Work History
American Carolina Clinical ResearchCharlotte, NC
Clinical Research Coordinator
01.2022 - Current
Job overview
- Coordinate all aspects of clinical site operations including patient recruitment, informed consent, eligibility verification, and data collection
- Maintain compliance with ICH-GCP, study protocols, SOPs, and sponsor requirements
- Conduct source documentation review and SDV in line with ALCOA-C principles
- Prepare and maintain essential regulatory documents for study start-up and maintenance
- Support investigator meetings, staff protocol training, and site initiation visits (SIVs)
- Ensure site’s readiness for monitoring visits, internal audits, and sponsor/FDA inspections
- Collaborate with cross-functional teams on AE/SAE reporting, data reconciliation, and CRF completion
- Utilize Veeva Vault and Florence for eTMF management and regulatory archiving
- Leverage EMR (Epic) and EDC tools (Oracle InForm, MedNet, BioClinical) to manage subject data
- Contribute to quality metrics tracking and timely resolution of monitoring queries
Pulmonary of the CarolinasCharlotte, NC
Front Desk Executive
04.2020 - 11.2021
Job overview
- Served as the first point of contact for patients, ensuring a warm and professional atmosphere leading to efficient check-in/check-out process for daily appointments
- Managed appointment scheduling, confirmations, and cancellations using Electronic Medical Records (EMR) systems
- Verified insurance eligibility, processed co-pays, and maintained accurate billing documentation
- Ensured HIPAA compliance through secure handling of confidential patient information
- Contributed to a patient-centered care by demonstrating empathy and professionalism
- Supported clinical staff by maintaining organized patient records, assisting with chart preparation, and coordinating daily schedules
Education
Abia State UniversityUturu, Nigeria
Bachelor of Arts from English and Literature Studies
05.2008
University Overview
Skills
- Clinical trial management (Phase I–III)
Certification
- Certified Scrum Master 2022
- ICH Good Clinical Practice (E6 R2) 2023
- Transporting Dangerous Goods Training 2024
- Pfizer Investigators Site Personnel ICH GCP 2025
- CSSR 2024
Hobbies and Interests
Hobbies and Interests
Networking, movies and reading
Availability
See my work availability
Not Available
Available
monday
tuesday
wednesday
thursday
friday
saturday
sunday
morning
afternoon
evening
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Accomplishments
Accomplishments
- Achieved [Result] by completing [Task] with accuracy and efficiency.
Languages
English
Native language
English
Proficient (C2)
C2
Work Preference
Work Type
Full TimePart TimeContract WorkWork Location
On-SiteHybridRemoteImportant To Me
Work-life balanceCompany CultureHealthcare benefitsWork from home optionPaid time offCareer advancementPaid sick leave401k matchTimeline
Clinical Research Coordinator
American Carolina Clinical Research
01.2022 - Current
Front Desk Executive
Pulmonary of the Carolinas
04.2020 - 11.2021
Abia State University
Bachelor of Arts from English and Literature Studies
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