Qi Zhang
HOUSTON
Summary
Highly skilled Clinical Trial Manager with strong background in overseeing all aspects of clinical trials, from planning to execution. Possess a deep understanding of regulatory guidelines and Good Clinical Practice (GCP). Strengths include strategic trial design, data management, and patient safety protocols. Previous roles have highlighted ability to optimize resources for efficient operation of clinical trials and successful attainment of research objectives.
Overview
8
8
years of professional experience
Work History
Clinical Trial Manager
Sanglin Biotech limited
Zhengzhou
08.2023 - Current
- Participated in meetings with sponsors, CROs, investigators, regulatory agencies concerning ongoing projects.
- Coordinated activities between internal staff members, vendors and third party contractors involved in the execution of clinical trials.
- Monitored progress of clinical trials, identified problems and developed solutions to ensure timely completion of studies.
- Presented updates about ongoing studies at internal team meetings and other relevant forums.
- Developed and implemented clinical trial management plans, protocols and reports.
- Created detailed timelines for each project to ensure milestones were met on schedule.
- Served as a liaison between sponsors, CROs, investigators, regulatory agencies when necessary.
- Evaluated potential new sites for participation in clinical trials based on their qualifications.
Research Professor
Zhengzhou University
Zhengzhou
02.2017 - Current
- Prepared reports summarizing results of research projects.
- Evaluated student performance through written assignments, exams, presentations.
- Organized workshops, seminars, symposia, and colloquia related to the field of study.
- Served on committees that reviewed proposals for funding new research initiatives.
- Developed and implemented research protocols for data collection, analysis, and interpretation.
- Participated in recruitment activities aimed at attracting qualified graduate students.
- Reviewed manuscripts submitted by colleagues for publication in scholarly journals.
- Analyzed and interpreted quantitative and qualitative data from experiments or surveys.
- Reviewed grant applications submitted by peers seeking funding for their own research projects.
Education
Master of Science - Pharmacology
West China Medical Center, Sichuan University
Chengdu07-2000
Skills
- Clinical trial management
- Protocol development
- Regulatory compliance
- Data analysis
- Project coordination
- Research methodology
Timeline
Clinical Trial Manager
Sanglin Biotech limited
08.2023 - Current
Research Professor
Zhengzhou University
02.2017 - Current
Master of Science - Pharmacology
West China Medical Center, Sichuan University
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