Dillon Dang
Orlando
Summary
Accomplished Clinical Research Assistant with a proven track record at Rare Disease Research, adept in patient recruitment and ensuring compliance with pharmaceutical sponsor guidelines. Excelled in facilitating clinical trials, demonstrating exceptional organizational skills and a deep understanding of federal regulatory compliance. Skilled in specimen handling and fostering patient education, significantly contributing to research accuracy and efficiency.
Overview
1
1
year of professional experience
Work History
Clinical Research Assistant
Rare Disease Research
06.2021 - 08.2022
- Educated patients regarding all facets of clinical study participation.
- Assisted with research protocol development.
- Demonstrated advanced knowledge of federal regulatory compliance guidelines.
- Managed updates and input for patient information database.
- Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
- Followed informed consent processes and maintained records.
- Participated in initiation visits and investigator meetings, implementing trials following study timelines and budgets.
- Gathered, processed, and shipped lab specimens.
- Maintained compliance with protocols covering patient care and clinical trial operations.
- Screened patient records, databases, and physician referrals to identify prospective candidates for research studies.
- Maintained accurate and up-to-date case report forms and source documents for traceability.
- Collaborated with clinical staff and other healthcare professionals to support clinical trial data accuracy.
- Prepared and maintained regulatory documents for clinical trial submissions.
- Monitored patient safety throughout clinical trials and reported any adverse events.
- Followed clinical research protocols and conducted study visits in compliance with ICH/GCP and FDA regulations.
Education
M.D. - Medicine
Saint George's University
Grenada05-2026
Bachelor of Science - Public Health
University of South Florida
Tampa, FL05-2021
Skills
- Medication trials
- Study monitoring
- Pharmaceutical sponsor compliance
- Patient recruitment
- Specimen collection
- Specimen handling
- Pharmaceutical sponsor guidelines
- Ethics committee guidelines
- Good clinical practice
- Participant screening
Timeline
Clinical Research Assistant
Rare Disease Research
06.2021 - 08.2022
M.D. - Medicine
Saint George's University
Bachelor of Science - Public Health
University of South Florida
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