Clinical research professional with experience as a Study Coordinator and Clinical Research Associate across multiple therapeutic areas. Skilled in clinical operations, study start-up, with a strong understanding of clinical trial execution.
Overview
5
5
years of professional experience
Work History
Sr. Clinical Research Associate
Syneos Health
In-House, CA
07.2026 - Current
Responsible for monitoring all types of clinical trials (Phase I-III); assures adherence to Good Clinical Practice, investigator integrity and compliance with all study procedures.
Primary responsibility is for site management and performance, including documentation. Site management activities include all in-house and on-site monitoring for all visit types: PSV, SIV, IMV, COV, etc.
Mentored and trained junior CRAs
Clinical Research Associate II
Syneos Health
In-House
06.2023 - 07.2026
Coordinated with multidisciplinary research teams to execute clinical trials for primarily, but not limited to, CNS research.
Partnered with Investigators, study coordinators, project managers, clinical trials manager, and cross-functional teams to support study start-up, enrollment, data quality, and study timelines.
Clinical Research Associate I
Syneos Health
In-House, CA
06.2022 - 06.2023
Participated in the global 6-week Clinical Training Institute (CTA) CRA program, which resulted in IAOCR (International accrediting Organization for Clinical Research) accreditation.
Conducted Site Initiation Visits (SIVs), Interim Monitoring Visits (IMVs), and Close-Out Visits (COVs), while performing study-related activities including investigational product (IP) accountability and drug reconciliation.
Clinical Research Coordinator
Collaborative Neuroscience Network, LLC
Garden Grove, CA
08.2021 - Current
Provided clinical support to assist PI, Sub-Is, and CRAs in all study related tasks, including patient eligibility, exams/visits, informed consent.
Assisted in the production of source documents to capture trial data.