Versatile clinical research professional knowledgeable about coordinating patient information, laboratory samples and compliance documents for diverse clinical trials. Highly organized and thorough with good planning and problem-solving abilities.
Overview
8
8
years of professional experience
1
1
Certification
Work History
Epic Clinical Research
02.2023 - Current
Managed all aspects of clinical research studies, including protocol development, participant recruitment, data management, regulatory compliance, and team coordination, to ensure successful study execution and advancement of scientific knowledge
Managed pharmacy responsibilities, in both a blinded and unblinded capacity, including mixing, verifying and administering medications
Protocol Management: Developed, implemented, and managed study protocols in collaboration with principal investigators, ensuring compliance with ethical and regulatory standards
Participant Recruitment and Screening: Actively recruited and screened eligible participants, maintained accurate records, and facilitated informed consent discussions to ensure study enrollment aligned with inclusion/exclusion criteria
Data Management and Compliance: Oversaw data collection processes, maintained meticulous documentation and ensured adherence to institutional review board (IRB) regulations, Good Clinical Practice (GCP) guidelines, and other regulatory requirements
Team Collaboration and Communication: Facilitated effective communication among multidisciplinary research team members, sponsors, regulatory authorities, and study participants to ensure smooth coordination of study activities and participant safety throughout the research process.
Administrative Assistant
Social Eyes Eye Studio
02.2022 - 02.2023
Conducted daily responsibilities of administrative assistant, performing the necessary medical testing
The coordination of sales with patient insurance benefits, insurance company and manufactures
The management of optical orders and inventory, with styling patients with eyewear, eyewear sales
By arranging the stock of eyeglasses, sunglasses, and accessories, you may maintain a neat and aesthetically pleasing daily optical display
Maintain proper relation with partnering medical offices and providers, conducting the insurance estimates.
Clinical Research Coordinator Program
VAST Clinical Research
04.2022 - 05.2022
Extensive Training on the following topics: Common Medical and Pharmacologic Terms Used in Clinical Research, Evolution and History of Clinical Research, Protection of Human Subjects in Clinical Research, ICH Good Clinical Practice, Therapeutic Areas in Clinical Research, FDA/EU regulations, IRB's, Informed Consent, Research Designs and Concepts, Site Coordination and Management, Clinical Research Coordinator Program - Externship
JCPENNEY
05.2019 - 01.2020
Maintain and organize online and inside orders
Tasked with conducting routine inventory checks, to ensure customer satisfaction
Ensured the work environment and store performance was adequate
Handle on average 200 online orders, same day pickups, returns and store exchanges equating to $10,000 per shift
Complete daily fulfillment report for two stock rooms containing 100 packages per room and audit 25 shortages per shift in a timely manner
Ranked top 10% for fulfillment orders in the third quarter of 2019 for the company by driving $125 or more of merchandise through online orders per month for the quarter.
Baybrooke Village Care and Rehabilitation
08.2016 - 06.2017
Tasked with the care of assisting residents with daily needs, medical procedures and dealing with the medical care to offer optimum level of care and comfort for each resident.
Education
Bachelor of Science in Anthropology -
Texas State University
Skills
Informed Consent Process
Investigational product management
Specimen collections
Clinical trial management
Certification
2022, VAST Clinical Research - Clinical Research Coordinator Program
2023, ICH E6 R2 - Good Clinical Practice, Global Health Network
2023, IATA- Transportation of Dangerous Goods , Mayo Clinic
Clinical Research Systems
EDC - Medidata Rave
IXRS - Cenduit
Knowledge Skills Abilities
Data Analysis of information, allowing for proper information gathering, along with problem solving.
Proper usage and understanding the Microsoft Teams, Microsoft Office (Excel, Word, PowerPoint).
Client/ Patient relations
Account Reconciliation to ensure the proper management of finances.
Senior Strategic Information Officer -CCCRN, State SI Lead at Centre for Clinical Care and Clinical Research NigeriaSenior Strategic Information Officer -CCCRN, State SI Lead at Centre for Clinical Care and Clinical Research Nigeria
Regional Director of Clinical Operations at KUR Research - Clinical Research Site NetworkRegional Director of Clinical Operations at KUR Research - Clinical Research Site Network