Detail-oriented, dependable clinical research professional aiming to leverage my knowledge in ICH/GCP Guidelines and increase an organization's operational efficiencies.
Overview
4
4
years of professional experience
Work History
Clinical Research Associate
ICON
Los Angeles, CA
09.2022 - Current
Reviewed and monitored sites to ensure compliance with ICH-GCP Local Laws. Audit/inspection readiness.
Verified timely completion and accuracy of subject data. Ensured site follow ALCOA Principles.
Monitored safety events reported during the course of clinical trials in accordance with SOPs and protocol.
Verified sites are following clinical trial protocol, study activities/assessments.
In-House Clinical Research Associate
ICON
Los Angeles, CA
07.2022 - 09.2022
Provided support to sites and CRAs directly to resolve queries and requests.
Contact clinical sites for requests including enrollment updates, missing documentation, action items, data entry timeliness and query follow-up.
Conduct and complete remote site management activities according to applicable SOPs and monitoring plan.
Clinical Research Coordinator
CalNeuro Research Group
Los Angeles, CA
01.2022 - 06.2022
Provide clinical research support to Principal Investigator for studies including OCD, PTSD, Depression, and Alzheimer's.
Collect, record, and maintain accurate subject study data according to study protocols.
Monitor subject safety and record any changes in medical history, medications or new adverse events.
Clinical Research Coordinator
Attune Health
Beverly Hills, CA
08.2020 - 12.2021
Worked with Principle Investigator and Sponsors to coordinate clinical trial activities for Autoimmune and Inflammatory studies involving Myositis, Osteoarthritis, Lupus.
Entered accurate subject data and resolved queries using electronic data capture systems including iMedidata, IBM, RedCap, RDC.
Assist with subject recruitment and schedule suitable subjects for screening visits.