Open to opportunities

Asia Spencer

@asiaspencer

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Seasoned Clinical Research Professional with extensive industry experience.

United States

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What I'm looking for

I am looking for a collaborative environment where I can contribute to innovative clinical research projects and further develop my skills.

I am a seasoned Clinical Research Professional with almost six years of experience in the industry. My journey has equipped me with a diverse skill set, including roles as a Clinical Research Associate, Clinical Trial Manager, and Research Consultant. I have successfully managed Phase I, II, and III trials across various therapeutic areas, including Veterinary, Pediatric, Neurological, and General Medicine. My expertise lies in ensuring compliance with Good Clinical Practices (GCP) and regulatory guidelines, while also fostering strong relationships with study sites and stakeholders.

Throughout my career, I have demonstrated my ability to lead teams and manage complex clinical trials. My recent role as a Clinical Trial Monitor at Ethos Discovery Veterinary Research involved overseeing project management, data integrity, and regulatory compliance. I have also contributed to the development of training materials and supported hospitals in onboarding for clinical trials. My commitment to quality and patient safety drives my work, ensuring that all research activities adhere to the highest standards.

I am passionate about advancing clinical research and continuously seek opportunities to enhance my knowledge and skills. I thrive in collaborative environments where I can contribute to innovative research solutions and support the development of new therapies. I am eager to bring my expertise to a dynamic team focused on making a positive impact in the field of clinical research.

Experience

Work history, roles, and key accomplishments

Current

Clinical Trial Monitor

Current

Ethos Discovery Veterinary Research

Nov 2024 - Present (7 months)

Performs set-up, maintenance, and close-out of project files and study information on Elligo and client systems. Manages projects for Discovery clinical trials to ensure timely delivery of high-quality work products. Coordinates team input to advance the research agenda and meet timelines, while also managing, editing, and reviewing trial documents.

Elligo Systems Project Management Power BI Protocol Deviations

Clinical Research Specialist/ Data Management

Encora Therapeutics

Jan 2024 - Oct 2024 (9 months)

Supported activities related to all phases of ET and Parkinson's, including regulatory, data, start-up, and maintenance. Managed and trained the study team on Clinical Research, EDC, eTMF, ISF, and Veeva. Monitored and evaluated research data for accuracy and compliance, conducting small audits to ensure compliance.

EDC ETMF ISF Veeva Patient Recruitment

CRA II/Clinical Trial Manager

Global Clinical Solutions

Jul 2022 - Jan 2024 (1 year 6 months)

Performed site qualification, interim monitoring, site management, and close-out visits ensuring regulatory and ICH/GCP compliance. Assessed factors affecting subject safety and data integrity, such as protocol deviations and pharmacovigilance issues. Routinely reviewed Investigator Site File (ISF) and Trial Master File (TMF) for accuracy, timeliness, and completeness.

ICH GCP TMF ISF Protocol Deviations Quality Control

Clinical Research Associate

IQVIA Biotech

Nov 2021 - Jul 2022 (8 months)

Participated in the preparation and execution of Phase I-IV clinical trials, overseeing progress and ensuring GCP compliance. Conducted study initiation activities, reviewed protocols, and provided training on study procedures, including the EDC system (Veeva Vault). Acted as the primary contact between IQVIA Biotech and investigators, performing study close-out visits and resolving outstanding ac

Clinical Trials GCP

Clinical Research Coordinator

Emory Healthcare/Children's Healthcare of Atlanta

Jan 2020 - Nov 2021 (1 year 10 months)

Developed, implemented, and supported the research process by assisting investigators in study design and data management specific to the subspecialty. Performed subject and guardian screening, enrollment, and study activities, coordinating study visits and procedures. Administered various research surveys, completed research-only testing, and ensured compliance throughout all study activities.

Research Design Data Management Source Documents Survey

Clinical Research Assistant

Mercer University

Jan 2019 - Jul 2022 (3 years 6 months)

Independently recruited and enrolled research subjects according to study protocols and university policies, checking eligibility criteria against medical records. Extracted data from university records and medical charts to complete case report forms with 99% accuracy. Managed assigned protocols and performed quality reviews of CRFs and records, ensuring compliance with FDA regulations and ICH/GC