Position: Clinical Trial Assistant/Research Assistant
Education:
Bachelor's or Master's degree in Pharmacy, Public Health, or related scientific fields.
Job Description:
1. Read and thoroughly understand the details outlined in the Protocol of each research project assigned and execute tasks accordingly.
2. Liaise with relevant departments such as Research Physicians and sponsors during the research process.
3. Prepare patients for screening/recruitment according to protocol specifications and timelines.
4. Assist and prepare clear and accurate consent documents for research participants during the Informed Consent process.
5. Ensure that patients receive scheduled eye examinations with the research physician as per protocol.
6. Facilitate and accommodate monitors during their visit for inspection.
7. Prepare documentation for reporting Adverse Events/Serious Adverse Events within both the hospital system and to the sponsor.
8. Collaborate with sponsors to ensure completeness and accuracy of various documents related to Amendments/Safety Reports for submission to the Institutional Review Board (IRB) for research approval.
9. Organize approved documents from IRB submissions into the Investigator Site File.
10. Study and understand the CRF recording for each project in detail.
11. Transfer data from source documents to CRFs (paper or electronic) within specified timelines.
12. Collect and forward specimens to the laboratory according to the research protocol.
13. Perform other duties as assigned by the Research Center Director.
Please send your CV to panadda.p@chulacrc.org.
"Clinical Trial Assistant" Recruit
