Abriana Gonzales
Mesa,AZ
Summary
Driven professional with experience in clinical research coordination, equipped to make significant impact in the medical field. Demonstrated ability to manage clinical trials, ensure compliance with protocols, and maintain accurate documentation. Strong emphasis on team collaboration, reliability, and adaptability to evolving project requirements. Proficient in patient recruitment, data collection, and regulatory submissions, with results-driven approach that ensures successful study outcomes.
Overview
5
5
years of professional experience
1
1
Certification
Work History
Clinical Research Coordinator III
HonorHealth
01.2025 - Current
- Spearheaded the development of the Rheumatology research department by implementing streamlined training materials, Study Patient List, and a Study Inventory Log to promote efficiency and rheumatology growth.
- Enhanced patient enrollment in clinical trials by developing and implementing effective recruitment strategies.
- Duties as outlined below in Oncology.
Clinical Research Coordinator III
HonorHealth
09.2024 - 01.2025
- Followed clinical research protocols and conducted study visits in compliance with ICH/GCP and FDA regulations.
- Screened patient records, databases, and physician referrals to identify prospective candidates for research studies.
- Led cross-functional team meetings to discuss trial progress and address any challenges, fostering collaborative work environment.
- Developed comprehensive database for tracking patient information, improving efficiency in data management.
- Facilitated clear communication between principal investigators, sponsors, and study participants for seamless trial execution.
- Developed training materials for new staff members, enhancing team competence and efficiency in clinical trial operations.
- Trained new team members on essential clinical research protocols and procedures, promoting a culture of continuous learning.
Clinical Research Coordinator II
HonorHealth
10.2022 - 09.2024
- Followed clinical research protocols and conducted study visits in compliance with ICH/GCP and FDA regulations.
- Enhanced patient safety by meticulously monitoring and documenting adverse events during clinical trials.
- Coordinated and monitored clinical trial activities to support timely and accurate completion of studies.
- Developed and maintained accurate and up-to-date case report forms and source documents.
- Oversaw ethical conduct of clinical trials, ensuring all activities were in accordance with ethical guidelines.
- Facilitated communication between research team and study sponsors, ensuring clear and consistent updates on trial progress.
Clinical Research Coordinator
Banner Health
01.2022 - 08.2022
- Assumed primary responsibility in the implementation and management of new clinical trials in a knowledgeable and collaborative manner.
- Provided study information and obtained relevant information to and from patients engaged in clinical studies, which included: assisting in the recruitment and screening of patients; registering patients; provided information on clinical trials and protocols to interested participants in a timely and helpful manner; collected previous relevant medical records data on patient; explained procedures and consent forms; updating databases with patient information, etc.
- Performed tasks required by protocol, which included obtaining patient medical history, systems review, phlebotomy, EKG, vital signs, and cognitive assessment on patients.
- Triaged adverse events and communicated with the research physician regarding the occurrence of adverse events.
- Served as a resource, educator, and support person for patients and families by being a consistent person they can contact within the clinical research program.
- Prepared appropriate IRB (Institutional Review Board) forms, informed consents, correspondence with sponsor, etc., in an accurate and timely manner.
Clinical Research Coordinator
ASU Biodesign Institute
05.2021 - 01.2022
- Established, set up, and maintained testing environments suitable for study type.
- Communicated with study participants, family members, and other contacts to provide study specific education.
- Coordinated and scheduled a variety of sample collections and laboratory tests.
- Developed and implemented recruitment strategies to attract ample participation.
- Coordinated the process for opening new studies and Ensured assigned studies were conducted in accordance with the Food and Drug Administration (FDA), Office for Human Research Protections (OHRP), Good Clinical Practices (GCP), and institutional guidelines.
- Oversaw subject enrollment, verifying and managing data and documentation in accordance to ALCOCA-C.
Clinical Research Technician - Shift Lead
ASU Biodesign Institute
08.2020 - 04.2021
- Supervised 4-member team by performing evaluations for each technician, training technicians on quality control, and reviewing results for verification and accuracy.
- Managed materials inventory and coordinated testing materials for COVID research.
- Used sound scientific procedures to create research samples and collect relevant data.
- Prepared experiments to test new research ideas, compiled raw data, and documented observations.
- Collaborated effectively with research team members to identify and solve issues impeding successful research.
- Organized and maintained the complete records for each study, including non-conformance reports, clinical inventory records, and regulatory paperwork.
Education
Bachelor of Arts - Anthropology
California State University, Chico
Chico, Ca05.2020
Skills
- Effective Interpersonal Communication, Teamwork, Cross-functional collaboration
- Adaptability
- Problem-Solving, Critical Thinking
- Statistical Data Analysis, Data management
- Effective Leadership
- GCP Guidelines, Phase I/II and IIT Clinical Trial Management, Feasibility Analysis
- Microsoft Excel, Microsoft Excel, Microsoft Powerpoint expertise
Certification
Certified Phlebotomist, 11/01/21-2023, Currently Renewing my Certification, Phlebotomy Training Specialists Mesa, Skillful and precise in performing venipunctures and capillary punctures; collecting, preparing, and storing blood samples.
CPR Certified 2025-2027
Personal Information Summary
Selflessness, empathy, and compassion are my greatest strengths as they have allowed me to grow in my knowledge and become a passionate healthcare provider.
Timeline
Clinical Research Coordinator III
HonorHealth
01.2025 - Current
Clinical Research Coordinator III
HonorHealth
09.2024 - 01.2025
Clinical Research Coordinator II
HonorHealth
10.2022 - 09.2024
Clinical Research Coordinator
Banner Health
01.2022 - 08.2022
Clinical Research Coordinator
ASU Biodesign Institute
05.2021 - 01.2022
Clinical Research Technician - Shift Lead
ASU Biodesign Institute
08.2020 - 04.2021
Bachelor of Arts - Anthropology
California State University, Chico
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