Focused Clinical Research Coordinator well-versed in study protocols, standard operating procedures and general trial oversight. Excellent problem-solving abilities with a detail-oriented nature. Ready to bring Four years of related experience to a challenging new role.
Overview
7
7
years of professional experience
Work History
Senior Clinical Research Coordinator
DM Clinical Research
Houston, TX
03.2022 - Current
Overseeing smooth running of clinical trails
Informing participants about study objectives
Monitoring research participants to ensure adherence to study rules
Adhering to research regulatory standard and ethical standards
Engaging with subjects and understanding their concerns
Maintaining detailed records of studies as per FDA guidelines, including items such as drug dispensation
Clinical Research Coordinator
Centex Studies Inc/ C-1 Headlands, LLC
Houston, TX
11.2020 - 03.2022
Comprehend study design of each protocol that is assigned
Perform procedures in compliance with study protocol
Recruit and screen study subjects according to specific protocol requirements
Collect and record study data in source documents via electronic system (CRIO)
Manage study related activities
Adherence to protocol requirements
Review laboratory data
Assess and document compliance
Manage investigational product
Assess, record, and report Adverse Events as outlined in specific protocol
Fresh Food Associate
Walmart
Friendswood, TX
11.2019 - 09.2020
Unloaded produce trucks and broke down produce pallets to organize produce within refrigerator and dry storage areas.
Scanned shelves and product cases for expired stock and outdated items.
Verified proper merchandising for freshness and quality of goods by properly handling produce, minimizing damage and spoilage of products.
Refilled and rotated items on shelves to maintain well-stocked inventory.
Assisting customers in ordering cakes, fulfilling deli orders and finding the right produce
Data Entry Clerk
Meador Staffing Solutions (Lyondellbasell)
La Porte, TX
02.2019 - 07.2020
Scan Certificate of Analysis and organize electronic database
Create excel spreadsheet for all finished goods and quality tests performed
Sort and organize documents into binders after scanning into computer file system
Create Certificate of Analysis for customers
Book product pounds in the JBA system
Research Coordinator
Vandeventer Research Place Foundation
St Louis, MO
11.2015 - 10.2018
Performed duties and responsibilities on four complex human clinical trials.
Coordinates with Principal Investigators, and central administration to help ensure that clinical research related activities are performed in accordance with Federal regulations.
Conducts informed consent process including interactions with HRPO (IRB) and discussions with research participants, including answering any questions related to studies.
Screens subjects for eligibility using protocol specific inclusion and exclusion criteria.
Maintains adequate inventory of study supplies.
Retains all study records in accordance within requirements.
Entered data into RedCap, modeled results and generated reports.