• Coordinate and support the day-day operations of multiple investigator initiated and industry sponsored phase III and IV clinical trials, ensuring adherence to protocols, GCP, applicable regulations, and SOPs. • Manage, educate, and communicate with research participants; obtain and document informed consent; conduct site visits per schedule of events and efficiently complete Case Report Forms ensuring ALCOA +• Manage and organize essential documents and maintain regulatory binders; prepare documents for IRB submission in compliance with regulatory requirements.• Collaborate cross-functionally and communicate effectively with all team members- including investigators, sponsors, statisticians, and pharmacists; keep team on target towards successful execution of all trial deliverables and milestones.

• Helped team with implementing and managing the day to day operations and tasks for multiple industry sponsored phase II and phase III Cardiovascular clinical drug trials.• Conducted and documented patient recruitment, informed consent, and participant study visits; maintained subject binders and study binders; and processed & shipped biological specimens in strict compliance with protocols, ICH guidelines and GCP (Good Clinical Practice), regulatory requirements, ethical standards, and institutional SOPs.

Served as group leader/coordinator for the Brown General Surgery Society, a student interest group with ~60 members. Worked closely with two colleagues (co-leaders) and the Faculty Physician group advisor. • Worked collaboratively with team to plan and manage all aspects of monthly panel, lecture, and robotic surgery workshop events; Identified and contacted Professionals to collaborate on or participate in events.• Attended monthly team meetings- reviewed overall progress, solving any issues identified; brainstormed, planned, and managed innovative, strategically aligned professional development initiatives.

Coordinator and Board Member of a student service group which partners with Clinica Esperanza, a community free clinic, and supports increasing healthcare access and improving health outcomes in the community. • Oversaw all aspects of the biweekly Neurology Clinic- planned schedule, managed patient list, and prepared visit documents; streamlined clinic workflow and served as a valuable liaison between patients and doctors.• Led monthly leadership meetings; facilitated effective team communication and collaboration- streamlining our decision-making process and driving forward high-quality process improvement initiatives.

• Worked on Neurology research focused on acute stroke, as a member of the Neurocritical Care Clinical Research team; Chosen by PI to manage a cohort study assessing clinical outcomes of prolonged CSF drainage in patients with aneurysmal Subarachnoid Hemorrhage. • Worked closely with PI, learning how to perform a clinical research study from study design and planning, to interpretation and reporting of data; Ensured key deliverables and study milestones were achieved on target and correctly, driving forward study successful execution. • Partnered with PI and Biostatisticians to perform statistical analysis and interpretation of data.• Wrote abstracts reporting results and presented research findings to the scientific community at the American Heart Association International Stroke Conference & American Academy of Neurology annual meeting, reaching large audiences world-wide.

• Managed multiple aspects of programs and events for the New Scientist Program, including peer mentoring and group tutoring programs, and biweekly panels and events, in support of DEI efforts to increase representation of STEM concentrators at Brown.• Designed and promoted digital marketing materials on social media and wrote engaging email newsletters; Increased event attendance by 60% and increased program participation by 40%.

• Worked on NIH funded pre-clinical studies, investigating a novel therapeutic agent for perinatal hypoxic-ischemic stroke, as a member of the Perinatal Brain Research Laboratory and under the direct supervision of the Research Laboratory Manager. • Conducted laboratory experiments and animal studies in compliance with protocols, Good Laboratory Practice (GLP), and IACUC guidelines; commended for achieving exceptional efficiency, accuracy, and precision.