Jennifer Silva Chávez
Mexico
Summary
Clinical research professional with experience in supporting clinical trials, ensuring compliance, and maintaining accurate documentation. Strong focus on team collaboration and achieving results, adaptable to changing needs. Skilled in regulatory requirements, data management, and patient coordination. Reliable with excellent organizational skills, contributing to successful project execution.
Overview
2
2
years of professional experience
Work History
Clinical Trial Assistant
ICON Plc
05.2024 - Current
- Support project teams in setting up, organizing, and maintaining clinical study documentation (e.g., Study Files, CRFs) and ensuring compliance with ICH GCP, ICON SOPs, and client systems.
- Assist in processing, logging, tracking, and quality control of Data Collection Forms.
- Conduct quality control audits to maintain inspection-ready study files.
- Coordinate trial material ordering, dispatch, and tracking (e.g., CRFs, lab supplies, drug supplies).
- Update Clinical Trial Management Systems to track study progress.
- Facilitate site communication, including enrolment updates and meeting arrangements.
- Assist with meeting coordination, agenda creation, and meeting minutes.
- Provide support in study-related payments, tracking reports, and training activities.
- Assist in the management and maintenance of the Trial Master File (TMF), ensuring all clinical trial documentation is accurately filed, organized, and compliant with regulatory standards.
Thesis Student Assigned to Biochemistry
Instituto Nacional De Cardiología "Ignacio Chávez"
01.2023 - 01.2024
- Performed protein purification using Immobilized Metal Affinity Chromatography (IMAC).
- Conducted molecular analysis via Western Blot and applied various protocols to assess cell viability and inhibition.
- Handled tumor and non-tumor cell lines, as well as animal models, for biological sample processing.
- Utilized molecular biology techniques and conducted molecular docking using AutoDock Vina.
- Applied fluorometric and colorimetric methods for determining enzymatic activities and solution concentrations.
- Managed laboratory equipment and materials for ongoing research projects.
Assisting in Biosensors Laboratory
Facultad De Medicina
06.2023 - 12.2023
- Contributed to projects focused on developing new antidiabetic drugs targeting proteins such as PTP1B and alpha-glucosidase.
- Assisted in the handling of pharmacological laboratory equipment and materials for ongoing research.
- Supported the laboratory team in research activities related to the discovery of novel therapeutic approaches.
Education
Bachelor of Science - Medicinal And Pharmaceutical Chemistry
Facultad De Quimica
Mexico, ME06-2023
Skills
- Electronic data capture
- Informed consent process
- Regulatory submissions
- Adverse event reporting
- Site monitoring
- Clinical trial management
- Clinical research ethics
- Patient recruitment
- Clinical study reports
- Fluent in english
- Auditing techniques
- Site selection
- Data management
- Study coordination
- Biostatistics
- Clinical operations
Accomplishments
- Applied knowledge of ICH GCP and regulatory guidelines to perform tasks in accordance with industry standards.
- CTA hub supervised team of 4 staff members.
- Achieved site activation through effectively helping with adding staff into different platforms.
- Assisted with data collection, tracking, and quality control, ensuring reliable and accurate data entry
Languages
German
Limited Working
English
Native or Bilingual
Spanish
Native or Bilingual
Timeline
Clinical Trial Assistant
ICON Plc
05.2024 - Current
Assisting in Biosensors Laboratory
Facultad De Medicina
06.2023 - 12.2023
Thesis Student Assigned to Biochemistry
Instituto Nacional De Cardiología "Ignacio Chávez"
01.2023 - 01.2024
Bachelor of Science - Medicinal And Pharmaceutical Chemistry
Facultad De Quimica
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