
- Preparation of patient pre-screening documents using inclusion and exclusion criteria from study protocol.
- Conducting thorough patient interviews to educate them on clinical trials and determine eligibility.
- Organizing and maintaining patient data in compliance with HIPAA and IRB regulations.
- Acting as Study Matter Expert (SME) on trial indications and creating educational materials to assist recruitment team.
- Connecting qualified patients with research sites and coordinating appointments, transportation and other logistics.
Electronic health records system (EHR)
Patient information management
Good clinical practices
Informed Consent
Student Outreach Team Lead - American Medical Students Association (AMSA) Roseau, Dominica - 2015-2017
Health Promotion Volunteer -The Loretto Hospital Chicago, USA- 2018-2019
COVID-19 Community Engagement Volunteer- Milton Cato Memorial Hospital, St Vincent and the Grenadines -2020-2021
Women’s Health Education Volunteer - Herbode- Educate a Girl Child Initiative NGO -2023- Present