Victoria Rico
Los Angeles,CA
Summary
Experienced clinical research professional with 7+ years of experience and significant expertise in overseeing complex projects and ensuring timely delivery while prioritizing patient safety. Skilled in strategic planning, budget management, and risk assessment. Strong focus on team collaboration, fostering results-driven environment, and adapting to changing needs. Known for reliability, leadership, and effective communication.
Overview
7
7
years of professional experience
1
1
Certification
Work History
Clinical Trial Project Manager
Advenchen Laboratories, LLC.
09.2023 - Current
- Oversees and helps manage all aspects of multiple phase I-III oncology clinical trials in accordance with FDA/ICH/GCP regulations
- Identifies, selects, and manages CROs and other third party vendors
- Participates in study start up procedures and budget negotiations
- Contributes to medical writing and preparation of protocols, ICFs, study manuals, and other related documents
- Manages CRAs and project-related tasks to ensure timelines are met
- Assists with pharmacovigilance tasks such as SAE report review and processing
Clinical Research Associate I/II
ICON, plc.
02.2022 - 08.2023
- Conducted initiation, monitoring and closeout visits to verify study procedures, regulatory documents and data completion
- Reviewed clinical data, source documentation, case report forms and investigative site regulatory files to verify accuracy and completion
- Liaised with clinical investigator to identify, assess and resolve site performance, quality and compliance issues
Research Associate II
Kaiser Permanente
06.2019 - 01.2022
- Coordinated the day-to-day activities of several small and large scale clinical research trials
- Assisted and oversaw quality assurance of study activities (i.e. data collection and validation, recruitment, biospecimen management, chart review and documentation)
Clinical Research Coordinator
Center for Clinical Trials of San Gabriel
06.2017 - 05.2019
- Supported, facilitated and coordinated the daily clinical trial activities playing a critical role in the conduct of the study
- Screened patient records, databases, and physician referrals to identify prospective candidates for research studies
- Coordinated with Principal Investigator and multidisciplinary departments to help ensure that research activities were performed in accordance with federal regulations and sponsor policies and procedures
Education
Master of Science - Health Policy and Mgmt.
Mount Saint Mary's University
Los Angeles, CA01.2019
Bachelor of Arts - Health Administration And Policy
UM Baltimore County
Baltimore, MD01.2015
Skills
- Project Management
- Stakeholder Communications
- Budgeting and forecasting
- Vendor Sourcing
- Coaching and Mentoring
- Pharmacovigilance oversight
- Protocol development
- ICH/GCP adherence
Certification
- SOCRA CCRP (2024)
- ICH/GCP (2023)
Timeline
Clinical Trial Project Manager
Advenchen Laboratories, LLC.
09.2023 - Current
Clinical Research Associate I/II
ICON, plc.
02.2022 - 08.2023
Research Associate II
Kaiser Permanente
06.2019 - 01.2022
Clinical Research Coordinator
Center for Clinical Trials of San Gabriel
06.2017 - 05.2019
- SOCRA CCRP (2024)
- ICH/GCP (2023)
Master of Science - Health Policy and Mgmt.
Mount Saint Mary's University
Bachelor of Arts - Health Administration And Policy
UM Baltimore County
Similar Profiles
Ella ChoiElla Choi
HR/ Admin Assistant at GenBody America LLC. (Kwell Laboratories LLC.)HR/ Admin Assistant at GenBody America LLC. (Kwell Laboratories LLC.)
Dylan MonteiroDylan Monteiro
Human Resources Administrative Assistant at Gaming Laboratories International, LLCHuman Resources Administrative Assistant at Gaming Laboratories International, LLC
Jashawnia TaplettJashawnia Taplett
Data Entry Specialist at Physicians Group Laboratories LLCData Entry Specialist at Physicians Group Laboratories LLC