CHELSEE' BELLAMY
Wilmington,NC
Summary
As an experienced Clinical Research Associate, I am well-versed in adhering to study protocols, standard operating procedures, and good clinical practices. With a keen eye for detail, I excel in problem-solving. With over four years of experience in the field, I am ready to take on a fast-paced role. My certifications include Clinical Trials Network Good Clinical Practice (CTN GCP), ICH GCPs, and Medidata Rave. I have a strong proficiency in MS Office and quickly adapt to new software. Specifically, I am skilled in Microsoft Word, Excel, and Office. Demonstrating enthusiasm and professionalism, I possess key skills in effective time management, critical thinking, strong work ethic, and being a valuable team player. I am highly skilled in communication and organization, paying meticulous attention to detail. Handling multiple tasks efficiently is a proven strength of mine. Additionally, I have exceptional interpersonal skills and provide exceptional customer service, complemented by solid organizational and time management abilities.
Overview
5
5
years of professional experience
Work History
CLINICAL RESEARCH ASSOCIATE
PPD, Thermo Fisher
Wilmington, NC
04.2021 - Current
- Act as the primary site contact for a phase II clinical trial, assessing study site conduct and compliance through site communication
- Perform site management and related activities on assigned projects, adhering to approved protocols, ICH-GCP guidelines, regulations, and SOPs
- Collect study documentation, resolve issues, and obtain outstanding information as required
- Develop and maintain collaborative communication with site staff
- Liaise with internal staff to collect documents, review data points, and analyze findings from EDC and file reviews.
- Experience in managing Institutional Review Board (IRB) submissions, ensuring compliance with ethical standards and regulatory requirements
MONITOR TECHNICIAN
New Hanover Regional Medical Center
Wilmington, NC
07.2020 - Current
- Monitor rhythms, document and interpret rhythm strips, and communicate rhythm changes to Licensed Care Provider
- Enter patient telemetry data into the computer system
- Respond appropriately to lethal and pre-lethal arrhythmias, reporting to nursing staff and assisting in Code Blue situations as needed
- Maintain expertise in monitoring equipment and utilize the computerized arrhythmia system for data collection
- Assist in performing routine EKGs on the cardiac telemetry unit.
CLINICAL RESEARCH/PROJECT MANAGEMENT INTERN
PPD, Thermo Fisher
Wilmington, NC
09.2019 - 04.2021
- Assisted team members with assigned tasks in specific project areas and completed tasks as per 'Student's Measurable Learning Objectives.' Received training within the department, attending departmental-specific training sessions
- Participated in meetings and other learning opportunities
- Performed additional tasks under the direction of the Global Project Management PPD supervisor.
Education
Bachelor of Science - Clinical Research
University of North Carolina At Wilmington
Wilmington, NC12.2021
Skills
- Database Management
- Training Proficiency
- Clinical Assessment Management
- Problem-Solving
- Regulatory Compliance
- GCP (Good Clinical Practice)
- Risk-Based Monitoring
- Site Management
- Specimen Handling
- Communication and Collaboration
Timeline
CLINICAL RESEARCH ASSOCIATE
PPD, Thermo Fisher
04.2021 - Current
MONITOR TECHNICIAN
New Hanover Regional Medical Center
07.2020 - Current
CLINICAL RESEARCH/PROJECT MANAGEMENT INTERN
PPD, Thermo Fisher
09.2019 - 04.2021
Bachelor of Science - Clinical Research
University of North Carolina At Wilmington
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