Dedicated and adaptable professional with a proactive attitude and the ability to learn quickly. Strong work ethic and effective communication skills. Eager to contribute to a dynamic team and support organizational goals.
Overview
11
11
years of professional experience
Work History
Clinical Data Analyst (Remote)
Symbio Proinnovera
Casselberry, USA
10.2022 - 09.2024
Review of study-specific protocols and annotated CRFs/eCRFs.
Perform in-depth clinical data review of study patient information to ensure complete and accurate data for analysis and protocol compliance.
Requires the ability to run data validation programs, identify and recommend program modifications, generate and track queries, and maintain protocol violation listings.
Write internal and external data queries for -based studies, and write and post manual queries within the EDC system.
Clinical Research Data Coordinator
Orlando Health Oncology Research
Orlando, USA
04.2022 - 10.2022
Data Entry Systems including Medidata Rave, Inform, Clincase, Medrio, and UCLA-EDC.
Assess and monitor patient response and adverse reactions.
Collaborate with physicians and other healthcare staff to ensure adherence to FDA and protocol guidelines.
Schedule and coordinate monitor visits for protocols.
Call and schedule survival follow-up visits for patients once they complete treatment in the study.
Assist the research team in preparing for site audits (sponsor and FDA).
Data Coordinator/Research Assistant
CNS Healthcare
Orlando, USA
08.2019 - 04.2022
EDC data entry systems include Medidata Rave, OpenClinica, Inform, and eClinical.
Perform Vitals, ECG, lab processing, and shipping specimens.
Administrative tasks include reviewing database call reports and visit reports.
Quality assurance for COVID-19 studies, including Pfizer, Novavax, and Janssen.
Clinical Research Lab Assistant
Orlando Immunology Center
Orlando, USA
05.2016 - 08.2019
Create lab kits for clinical trials, and organize lab kits.
Ordering lab kits and supplies for all clinical trials.
EDC data entry systems include Medidata Rave, OpenClinica, and Inform.
Processing and shipping of specimens.
Back up to the pharmacy, duties including receiving investigational drug and distributing it to study subjects.
Clinical Research Coordinator
Compass Research
Oviedo, USA
12.2013 - 04.2015
Coordinate and co-lead over 15 clinical trials, which include Type II Diabetes, Osteoarthritis, Testosterone, weight loss with Type II Diabetes, and Cardiovascular risk patients, smoking cessation, COPD, and Asthma.
Perform EKGs.
Process lab specimens and shipping.
Order and receive investigational drug, medical devices for all studies.
Monitor study activities to ensure compliance with all protocols and with all relevant local, federal, and institutional policies.
Education
Bachelor of Science - Health Service Administration
University of Central Florida
08.2013
Associates of Arts -
Valencia Community College
12.2010
Skills
Good clinical practice
Time management abilities
Problem-Solving
Team Collaboration
Critical Thinking
Data Analysis
Multitasking
Excellent Communication
Data Collection
Analytical Thinking
Quality Assurance
Clinical Research
Problem-solving abilities
Data Mining
Timeline
Clinical Data Analyst (Remote)
Symbio Proinnovera
10.2022 - 09.2024
Clinical Research Data Coordinator
Orlando Health Oncology Research
04.2022 - 10.2022
Data Coordinator/Research Assistant
CNS Healthcare
08.2019 - 04.2022
Clinical Research Lab Assistant
Orlando Immunology Center
05.2016 - 08.2019
Clinical Research Coordinator
Compass Research
12.2013 - 04.2015
Bachelor of Science - Health Service Administration