Eric Yu
Summary
Possessing a strong understanding of scientific principles and a genuine desire to advance in the clinical research field, I offer a valuable blend of knowledge and enthusiasm to contribute to your organization. Adept at adhering to regulatory guidelines and equipped with exceptional data entry and organizational abilities, I am well-equipped to navigate the intricacies of clinical research. Prepared to leverage and enhance my analytical and organizational skills in an Entry-Level Clinical Research Associate position, I aim to make a significant impact on your team.
Overview
5
5
years of professional experience
1
1
Certification
Work History
Clinical Trial Assistant
IQVIA
06.2023 - Current
- Assist Clinical Research Specialist (CRS)/In-house Clinical Research
- Specialist(iCRS), Clinical Research Associates (CRAs)/In-house Clinical
- Research Associate(iCRA) and Regulatory and Start-Up (RSU) with accurately updating and maintaining clinical systems that track site compliance and performance within project timelines
- Assist the clinical team in the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures
- Assist with periodic review of study files for completeness
- Assist CRS/iCRS, CRAs/iCRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information
- Assist with the tracking and management of Case Report Forms (CRFs), queries and clinical data flow
- Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation
- May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training and with required approval
- May perform assigned administrative tasks to support team members with clinical trial execution
- Streamlined clinical trial documentation by efficiently organizing and maintaining accurate records.
- Collaborated with cross-functional teams to enhance overall efficiency in clinical trial execution.
- Promoted patient safety by assisting with Adverse Event reporting procedures in accordance with regulatory requirements.
- Prepared comprehensive reports on clinical trial progress for periodic review meetings with stakeholders.
- Answered telephone calls to offer office information, answer questions, and direct calls to staff.
- Implemented care and efficiency improvements to support and enhance office operations.
Graduate Student Researcher
NTU CLSMB
06.2020 - 09.2022
- Collaborated with more than 10 academic colleagues on areas of shared research interest such as Cancer-Associated Thrombosis and Cancer Development .
- Interpreted and analyzed research data to draw conclusions on outcomes.
- Prepared fact sheets, tables, and graphs to summarize research results.
- Performed various assays to support research studies.
- Employed critical thinking skills when faced with unexpected challenges during experiments ultimately resolving issues without compromising integrity.
- Developed strong relationships with faculty members, enabling successful collaboration on various research projects.
Intern
Sofiva Gene, Ltd.
03.2020 - 06.2020
- Facilitated smooth laboratory operations through proactive troubleshooting and maintenance of sophisticated equipment.
- Reduced sample contamination risks by adhering to strict protocols in the preparation and handling of specimens.
- Collaborated with interdisciplinary healthcare teams for improved patient outcomes, sharing critical lab findings and insights.
- Kept laboratory in compliance with applicable guidelines and laws.
Medical Technologist Intern
National Taiwan University Hospital
07.2019 - 01.2020
- Contributed to the overall success of the laboratory by maintaining a positive attitude and demonstrating strong teamwork skills in daily interactions with peers.
- Followed laboratory protocols for specimen processing, analysis, and results reporting.
- Analyzed laboratory findings to check accuracy of results.
- Collected and reviewed patient medical histories to accurately interpret test results.
- Reduced turnaround time for test results by efficiently processing specimens and maintaining optimal instrument performance.
Education
Master of Science - Clinical Laboratory Science
National Taiwan University
Taipei, Taiwan09-2022
Bachelor of Science - Clinical Laboratory Science
National Taiwan University
Taipei, Taiwan06-2020
Skills
- Regulatory submissions
- Adverse event reporting
- Clinical trial management
- Clinical research ethics
- Drug safety monitoring
- Standard operating procedures
- Clinical study reports
- Auditing techniques
- Study coordination
- Study documentation
- Clinical data review
Certification
- Certified Medical Laboratory Technologist (MLT) - Ministry of Health and Welfare (HPA).
- EF SET English Certificate (82/100)-C2 Proficient-EF SET-2023
- TOEIC 915 (L:465/R:450)-ETS-2018
Languages
English
Bilingual or Proficient (C2)
Chinese (Mandarin)
Bilingual or Proficient (C2)
Courses
1. 藥物臨床試驗訓練課程(通過)-財團法人醫藥品查驗中心(Center of Drug Evaluation, CDE)-2023
2. 真實世界證據/真實世界數據 (RWE/RWD)訓練可成(通過)-財團法人醫藥品查驗中心(Center of Drug Evaluation, CDE)-2023
3. 臨床研究專員(CRA)專業實務訓練課程工作坊-財團法人生物技術開發中心(Development Center of Biotechnology, DCB)-2023
Timeline
Clinical Trial Assistant
IQVIA
06.2023 - Current
Graduate Student Researcher
NTU CLSMB
06.2020 - 09.2022
Intern
Sofiva Gene, Ltd.
03.2020 - 06.2020
Medical Technologist Intern
National Taiwan University Hospital
07.2019 - 01.2020
- Certified Medical Laboratory Technologist (MLT) - Ministry of Health and Welfare (HPA).
- EF SET English Certificate (82/100)-C2 Proficient-EF SET-2023
- TOEIC 915 (L:465/R:450)-ETS-2018
Master of Science - Clinical Laboratory Science
National Taiwan University
Bachelor of Science - Clinical Laboratory Science
National Taiwan University
Similar Profiles
Saravanan JSaravanan J
Associate Manager at IQVIAAssociate Manager at IQVIA
PITTS JARRELLPITTS JARRELL
Medical Technician at IQVIAMedical Technician at IQVIA
Sebastien BrockSebastien Brock
Business Process Analyst at IQVIABusiness Process Analyst at IQVIA