Intern
I'SHNOVA ClINICAL
09.2022 - 03.2023
- Followed clinical research protocols and conducted study visits in compliance with ICH/GCP and FDA regulations.
- Enhanced patient safety by meticulously monitoring and documenting adverse events during clinical trials.
- Followed informed consent processes and maintained records.
- Collaborated with clinical staff and other healthcare professionals to support clinical trial data accuracy.
- Developed and maintained accurate and up-to-date case report forms and source documents.
- Assisted in drafting comprehensive research reports summarizing findings, conclusions, and recommendations for further action.
