Jessica Woods
AL
Summary
Experienced Clinical Research Professional who graduated Summa Cum Laude with a Bachelor's in Health Sciences. Proficient in clinical trial planning and management, regulatory documentation, patient recruitment and retention strategies, as well as managing investigator payments. Proven ability to streamline communication between sponsors, CROs, and research study teams while ensuring compliance with Good Clinical Practices and regulatory standards.
Overview
14
14
years of professional experience
Work History
Clinical Trial Associate
Summit Clinical Research
01.2023 - Current
- Maximize efficiency and results by spearheading project management including obtaining project-specific statements of work, refining research protocols, solidifying requirements, establishing budgets, preparing forecasts, managing timelines, and directing timely execution
- Leverage a deep understanding of metabolic dysfunction-associated steatohepatitis (MASH) research to lead preparation, operations, protocol implementation, and Sponsor communication.
Clinical Research Specialist
Medtronic (Remote)
07.2020 - 01.2023
- Oversee, plan, develop, and execute clinical evaluation research studies
- Prepare protocols and patient record forms
- Carry out registered and non-registered clinical studies of various products determined to either satisfy medical needs or offer a commercial potential
- Coordinate with projects teams to oversee and resolve operational aspects of clinical trials in compliance with safety, regulatory, and legal procedures
- Devise clinical trial budgets and manage clinical supply chain operations.
Medical Scribe and Performance Coach
Yale New Haven Hospital (Remote)
07.2017 - 07.2020
- Provided detail and accurate description of patient's medical history as per electronic medical record regulations
- Enabled physicians in developing appropriate treatment plan by analyzing imaging, pathology, and other labs status, while accelerating patient dispositioning
- Enhance patient health outcomes and addresses needs via patient-centered-care; documenting patient's details
- Uncover and resolve issues, monetize services with policy enforcement, improve care quality via chart auditing, and lead over 35 scribes in compliance with HIPAA.
Aircraft Structural Maintenance
United States Air Force
08.2010 - 08.2016
- Delivered support to over $3.5B equipment and conducted inspections for mission critical aircraft's structural integrity, while implementing quick force deployment status
- Progressed mission capabilities by 70% on Southeast Pacific Command to ensure mission accomplishment, while minimizing reflection by revitalizing radar absorbent material on F-16.
Education
Master of Science - Clinical Research Administration
The George Washington University
Bachelor of Science - Health Sciences
Arizona State University
05.2019
Skills
- Research & Analysis
- Good Clinical Practices
- Lab Procedure & Protocol Knowledge
- Clinical Trial Planning & Management
- Regulatory Documentation Collection & Submission
- Patient Recruitment & Retention
- Investigator Payments
- eTMF Management
- Electronic Data Capture
- Microsoft Office
- Teamwork and Collaboration
- Attention to Detail
Timeline
Clinical Trial Associate
Summit Clinical Research
01.2023 - Current
Clinical Research Specialist
Medtronic (Remote)
07.2020 - 01.2023
Medical Scribe and Performance Coach
Yale New Haven Hospital (Remote)
07.2017 - 07.2020
Aircraft Structural Maintenance
United States Air Force
08.2010 - 08.2016
Master of Science - Clinical Research Administration
The George Washington University
Bachelor of Science - Health Sciences
Arizona State University
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