Summary
Overview
Work History
Education
Skills
Certification
Languages
Timeline
Generic

FELICIA HOCKODAY

Fort Worth,TX

Summary

Diligent Clinical Research Coordinator with comprehensive background in coordinating clinical research studies. Successfully managed multiple clinical trials from initiation to closeout, ensuring adherence to regulatory guidelines. Demonstrated ability to effectively communicate with cross-functional teams and maintain meticulous documentation.

Overview

7
7
years of professional experience
1
1
Certification

Work History

Clinical Research Coordinator, Clinic Lead

HD Research
02.2022 - Current
  • Responsible for all aspects of coordinating clinical trials
  • Screen patient records, databases, and physician referrals to identify prospective candidates for research studies.
  • Obtains informed consent
  • Provides review and input on source documents
  • Request, obtain and review patient’s medical records
  • Performs all study related procedures
  • Communicates with other study personnel including site staff, monitors, sponsor and CRO personnel; prepares for and participates in study visits with monitors and study auditors
  • Reports AE/SAE
  • Train new team members on essential clinical research protocols and procedures, promoting a culture of continuous learning.
  • Conducts comprehensive reviews of clinical trial protocols to identify and rectify potential issues before study initiation.
  • Updates in EDC
  • Resolves queries
  • Prepare for activities associated with audit and regulatory inspection
  • Follows clinical research protocols and conducted study visits in compliance with ICH/GCP and FDA regulations
  • Order and maintain study specific supplies


Clinical Research Coordinator II

ACRC Trials
04.2021 - 02.2022
  • Worked closely with Principal Investigator and other staff on implementing clinical trials
  • Coordinated the day-to-day activities of the designated studies
  • Followed clinical research protocols and conducted study visits in compliance with ICH/GCP and FDA regulations.
  • Maintained regulatory binders, CRF's, and source documents
  • Interacted with IRB personnel for study status
  • Screened patients for eligibility and enrolled eligible subjects
  • Lead client protocol discussions where appropriate in order to mitigate risk, considering the logistics, safety (staff and participants), and site’s capabilities
  • Inventoried and dispensed investigational products
  • Worked with study personnel including site staff, monitors, sponsors and CRO personnel from SMV to study close-out visit
  • Interacted with patients from enrollment and throughout the study trial
  • Gathered, processed, and shipped lab specimens.
  • Enhanced patient safety by meticulously monitoring and documenting adverse events during clinical trials.
  • Reduced data entry errors by implementing stringent quality control measures throughout the study lifecycle.

Clinical Research Coordinator I

LabCorp Drug Development
09.2018 - 02.2021
  • Worked closely with Principal Investigator and other staffs on implementing clinical studies
  • Facilitated and attended all key Study Planning meetings
  • Trained new team members on essential clinical research protocols and procedures, promoting a culture of continuous learning.
  • Performed all aspects of the set-up process to include the development and approval of study specific documents, schedules, and clinical procedure planning
  • Obtained informed consent, Patient’s demographics and MH
  • Verified study eligibility and study enrollment requirements according to the protocol
  • Collected, processed and shipped samples per protocol/IATA training
  • Updates in EDC
  • Completed all study related activities meeting SOP and protocol deadlines
  • Collaborated with clinical staff and other healthcare professionals to support clinical trial data accuracy.
  • Coordinated with cross-functional teams to ensure timely completion of clinical trial milestones.

Education

Associate of Applied Science - Medical Laboratory Science

Grayson College
Denison, TX

Skills

  • Good clinical practices (GCP)
  • Electronic data collection
  • Documentation management
  • Informed consent
  • Study protocols
  • Patient recruitment
  • Investigational product management
  • Phlebotomy
  • Specimen collections
  • Specimen handling
  • Critical thinking
  • Medical terminology

Certification

  • IATA
  • BIO Safety
  • HIPPA
  • GCP
  • GDP
  • CITI Training
  • Phlebotomy Certificate


Languages

English
Native or Bilingual

Timeline

Clinical Research Coordinator, Clinic Lead

HD Research
02.2022 - Current

Clinical Research Coordinator II

ACRC Trials
04.2021 - 02.2022

Clinical Research Coordinator I

LabCorp Drug Development
09.2018 - 02.2021

Associate of Applied Science - Medical Laboratory Science

Grayson College

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