At Wharton Medical Clinical Trials, I managed participant recruitment, informed consent, visits, and follow-up across clinical studies. I collected and reviewed eCRF data, maintained source documentation, and tracked missing data and protocol deviations.
As Senior Clinical Research Coordinator, I led day-to-day delivery of concurrent Phase II-IV industry-sponsored studies. I oversaw source-document and eCRF quality, coordinated study start-up and ethics submissions, and supported safety follow-up and inspection readiness.
At Western University, mentored by Novartis, I designed and executed a systematic review of Canadian real-world studies evaluating psoriasis biologics. I built an evidence-screening dataset covering 538 records and applied ROBINS-I and GRADE principles to assess evidence quality. Earlier, as a Medical Science Liaison at Exphar, I translated clinical evidence into scientific reports and supported observational studies and post-marketing initiatives.
