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
3
3
years of professional experience
Work History
Clinical Research Coordinator
Paradigm Clinical Research
02.2023 - Current
Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
Collected data and followed research protocols, operations manuals, and case report form requirements.
Gathered, processed, and shipped lab specimens.
Monitored unit budget to meet financial objectives for spend rate and funding.
Clinical Research Coordinator
Cancer Clinical Trials Office, University of CO
05.2021 - 02.2023
Complied with market research best practices and appropriate GCP guidelines during each clinical study
Schedules, coordinates, and prepares for sponsor monitor visits/audits and patient appointments
Collected data and followed research protocols, operations manuals and case report form requirements
Screened patient records, databases and physician referrals to identify prospective candidates for research studies.
Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
LAB ASSISTANT
01.2021 - 05.2021
Inform Diagnostics
Organized and ran tests on COVID samples and data from over 500
samples per day
Led a team in accessioning data from one form of software to another
software form
Managed and strategically planned input and output inventory of COVID
samples
Assisted with support duties such as filling products, labeling products,
testing samples and taking inventory.
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