Caitlyn Tse
Huntington Beach,CA
Summary
Clinical research professional with 2 years experience in Clinical monitoring, study management, and site initiation. Experience in Dermatology, Cardiology, and Trauma clinical trials. History of biomedical laboratory and oncology research. History of science and medical journal article review, editing, and publication. Detail and results oriented with excellent problem solving and communication skills.
Overview
4
4
years of professional experience
Work History
Clinical Research and Laboratory Associate
Keck School Of Medicine Of USC
05.2023 - Current
- Participates in Investigator and other external or internal meetings as required and communicates with other clinical associates and sites regarding data evaluation and site issues.
- Help facilities inspection and collection of regulatory documents, specifically utilizing RedCap and EXCEL for data entry in compliance with HIPAA and GCP.
- Collaborates with site staff during initiation visits on establishing site recruitment plan.
- Reviews site-level data in clinical systems, evaluates data quality issues, and establishes best methods for data entry and evaluation for large scale multi-center clinical trials.
- Assisted in developing IRB proposal drafts through iStar.
- Performs several biological assays including q-PCR, western blot, mouse handling, cell culture, to identify effects of CD200, an immunological agent, on its effects on tumorigenesis and malformation in mouse populations.
Clinical Research Coordinator/Medical Assistant
SCARS Center
08.2022 - 05.2023
- Served as primary in-house contact for Principal Investigators (PIs) and clinical research staff.
- Prepared site for research patient visits and gathered patient recruitment data.
- Reviewed site-level data in clinical systems and ensured timely, high quality data entry compliance.
- Collected updated/amended regulatory documents, identified site issues regarding documentation, communication, and training and recommends solutions.
- Ran and facilitated several study visits with over 50+ patients at a high volume dermatology office as a part of my mixed medical assistant position.
- Prepared and collected essential regulatory documents for review and approval during site start-up.
- Assisted as a back office medical assistant gathering patient intake, presenting to physicians, assisting in several dermatology office procedures such as MOHS, excisions, biopsies, etc.
Clinical Research Assistant
University Of Michigan
08.2021 - 08.2022
- Initiated all study visits and managed data collection and participant recruitment.
- Submitted all IRB materials in accordance with ICH GCP guidelines.
- Ran clinical trials studying the efficacy of a commercial board game in identifying motor deficits in a healthy cohort of patients.
- Managed data entry, submission, and transmission between the University campus and the University of Michigan hospital under HIPAA guidelines.
- Worked with clinical research team to run meetings and make sure site was running efficiently.
- Correct any site errors virtually and train additional clinical research staff on protocols for study initiation and visits.
- Created presentations, posters, and papers for publication and managed all data graphics and submissions.
Clinical Research Coordinator/Medical Assistant
Children's Cardiology Group
08.2020 - 08.2022
- Drafted and collected necessary regulatory documents for study implementation at a high volume cardiology practice.
- Drafted and revised several cases for publication in journals such as JACC, CASE, etc.
- Worked as a back office medical assistant obtaining vitals and scribing for physicians.
- Assisted with central and local Institutional Review Board/ethics committee submissions.
- Helped manage financial budget and billing for the practice.
Education
Certificate - CITI Good Clinical Practices
Keck School of Medicine USC
Los Angeles, United States2023
Bachelor of Science - Kinesiology
University of Michigan - Ann Arbor
Ann Arbor, MI2022
Skills
Microsoft Office
Microsoft EXCEL
EHR Systems
Medical terminology
Self motivated
- Strong planning skills
- Technical expertise
- Public speaking
- Detail-oriented
Telecommunication skills
Skills
Microsoft Office, Microsoft Windows, EHR Systems, Safety Reporting, Medical Terminology, Good Documentation Practice, ICH-GCP
Timeline
Clinical Research and Laboratory Associate
Keck School Of Medicine Of USC
05.2023 - Current
Clinical Research Coordinator/Medical Assistant
SCARS Center
08.2022 - 05.2023
Clinical Research Assistant
University Of Michigan
08.2021 - 08.2022
Clinical Research Coordinator/Medical Assistant
Children's Cardiology Group
08.2020 - 08.2022
Certificate - CITI Good Clinical Practices
Keck School of Medicine USC
Bachelor of Science - Kinesiology
University of Michigan - Ann Arbor
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