Will Odom
Wilmington
Summary
Clinical Research Associate with a focus on oncology trials. Having managed over seven large-scale, multi-center trials, and specializing in clinical trial management and GCP compliance. Demonstrated ability to enhance site performance through targeted training and effective problem-solving strategies. Proficient in report preparation and safety monitoring, ensuring successful study outcomes through strong collaboration.
Overview
7
7
years of professional experience
1
1
Certification
Work History
Clinical Research Associate
Thermo Fisher
Wilmington
01.2024 - Current
- Interacted with sponsors, CROs, investigators, vendors and subcontractors as needed.
- Analyzed collected data for accuracy prior to database lock; identified discrepancies when necessary.
- Managed relationships with external vendors such as laboratory services or imaging centers.
- Prepared reports summarizing study progress and results for senior management review.
- Provided training on GCP standards to new personnel or existing staff members.
- Performed clinical research activities including protocol development, subject recruitment and data collection.
- Ensured proper storage of investigational product at investigator sites per GCP guidelines.
- Tracked enrollment status across multiple sites to ensure target goals were met in a timely manner.
- Reviewed and monitored clinical trial sites to ensure compliance with Good Clinical Practices guidelines.
- Monitored safety events reported during the course of clinical trials in accordance with SOPs.
Remote Site Monitor
Thermo Fisher
Wilmington
07.2020 - 01.2024
- Performs all aspects of in-house site management in accordance with GCP, and acts as the primary contact for sites.
- Conducts regularly scheduled site management calls with study sites to support the sites’ execution of their study responsibilities.
- Responded to ad hoc site requests for assistance.
- Assisted with the resolution of data queries and provided ongoing site training. Performed a data review using EDC, in-house dashboards, and the CTMS system for reporting.
- Reviewed the site, essential documents, and participated in multiple local interim analyses.
Clinical Trial Coordinator
Thermo Fisher
Wilmington
07.2018 - 07.2020
- Performed project administrative tasks for clinical trials.
- Tracked and filed all documents, and supported project managers in project-related expenditures.
- Performed country and site file reviews, distributed country and site-level communications, and compiled and distributed investigator site file and pharmacy binders to sites.
Education
Bachelor of Science - Biology
University of North Carolina At Wilmington
Wilmington, NC05-2017
Associate of Science -
Brunswick Community College
Bolivia08-2015
Skills
- Clinical trial management
- Site monitoring
- Report preparation
- Subject recruitment
- Safety monitoring
- Risk Assessment and Root Cause Analysis
- Problem solving
- Team collaboration
- Training delivery
- Time management
- GCP compliance
- Effective communication
Certification
- Vaccines Academy Certificate Program, 2024
- CRA Academy, 2024
- Clinical Foundations Program, 2020
Timeline
Clinical Research Associate
Thermo Fisher
01.2024 - Current
Remote Site Monitor
Thermo Fisher
07.2020 - 01.2024
Clinical Trial Coordinator
Thermo Fisher
07.2018 - 07.2020
Bachelor of Science - Biology
University of North Carolina At Wilmington
Associate of Science -
Brunswick Community College
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