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The knowledgeable clinical research assistant is adept at recognizing clinical values and abstract data from source documents. Uses analytical skills to identify data or patient safety issues. A versatile clinical research professional is knowledgeable about coordinating patient information, laboratory samples, and compliance documents for diverse clinical
trials. Highly organized and thorough with good planning and problem-solving abilities. Certified in Taiwan. Skilled at collecting specimens, dispensing medications, and consulting with patients during the course of clinical research trials. Experienced in coordinating schedules, results, and documentation. Focused Clinical Research Coordinator well-versed in study protocols, standard operating procedures, and general trial oversight. Excellent problem-solving abilities with a detail-oriented nature. Ready to bring 2.2 years of related experience to a challenging new role.

Mackay Medical College

Chung Shan Medical University 

Clinical Research Associate

謝艾芸

CONMED PHARMACEUTICAL & BIO-MEDICAL CORPORATION.

Coordinated clinical trials focused on disorders such as uremic pruritus.
Manage the clinical trials：
– Integrative clinical trials in 9 sites to approve IRB, and responsible for team education training.
– Develop protocols, case reports, statistical analysis plans, and standard operating procedures to comply with the ICH/GCP.
-Corporate with SMO company to recruit and manage study nurses.
- Management of projects to ensure the adherence of the project to quality standards and the approved timeline and budget.

Coordinated clinical trials focused on disorders such 
 	 as CLI and OA. 
 	 Worked with principal investigator and sponsors to 
 	 facilitate daily trial activities and comply with 
 research protocols. 
 	 Followed informed consent processes and 
 maintained records. 
 	 Maintained compliance with protocols covering 
 	 patient care and clinical trial operations. 
 	 Participated in initiation visits and investigator 
 	 meetings, implementing trials in accordance with 
 	 study timelines and budgets.

Taiwan Bio Therapeutics

Coordinated clinical trials focused on disorders such as migraine, dementia, and AI software development.
Analyzed statistical data using both modern and traditional methods. 
Summarized search results by preparing written reports, graphs, fact sheets, and tables. 
Performed statistical, qualitative, and quantitative analysis. 
Collaborated with the leadership team to identify relevant questions and determine the best methods of collection.
Planned, modified, and executed research
techniques, procedures, and tests.
Conducted DNA, RNA, and protein extraction and
quantification using spectrophotometer and gel
electrophoresis.
Submitting IRB, explaining ICF to patients and visiting
patients.
 


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