Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
Participated in initiation visits and investigator meetings, implementing trials following study timelines and budgets.
Managed patient recruitment, informed consent process and data entry to support trial objectives.
Prepared and maintained regulatory documents for clinical trial submissions.
Reviewed referral information and kept track of intakes from various referral sources.
Searched at library and in scholarly databases to locate necessary information for research projects.
Clinical Research Assistant
Dr. Steven R Brant & Dr. Lea Ann Chen
09.2023 - 05.2024
Managed study databases, ensuring accurate data entry, storage, and retrieval for analysis purposes.
Maintained up-to-date knowledge of industry regulations by reviewing relevant publications regularly.
Developed strong relationships with patients through compassionate care coordination during their participation in clinical studies.
Expedited study progress by overseeing timely completion and submission of required documents, forms, and reports in accordance with regulatory guidelines.
Educated patients regarding all facets of clinical study participation.
Gathered, processed, and shipped lab specimens.
Followed informed consent processes and maintained records.
Screened patient records, databases, and physician referrals to identify prospective candidates for research studies.
Performed venipunctures
Collected blood samples using vacutainer tubes, tourniquets, syringes, butterfly needles, and straight needles.