Study Coordinator

Description The Department of Medicine is seeking a highly organized and detail-oriented Clinical Research Coordinator to support clinical research studies within the Division of Cardiology. In this role, you will oversee the day-to-day coordination of studies from start-up through closeout, ensuring compliance with study protocols, institutional policies, FDA regulations, and ICH Good Clinical Practice (GCP) guidelines.

Working collaboratively with investigators, sponsors, and multidisciplinary research teams, you will play a key role in advancing innovative clinical research while managing multiple priorities in an academic medical center. Hourly range: $36.37-$58.52 Qualifications Required: Bachelors Degree or 1-3 years of previous study coordination or clinical research coordination experience. Strong verbal and written communication skills along with strong interpersonal skills to effectively establish rapport, and build collaborate relationships.

Strong organizational capabilities to organize multiple projects and competing deadlines for efficiency and cost-effectiveness.. Analytical skills sufficient to work and solve address problems and identify solutions with reasoned judgment. Ability to adapt to changing job demands and priorities; work flexible hours to accommodate research deadlines.

Mathematical skills Sufficient to prepare clinical research budgets, knowledge of math ability and knowledge of clinical trials research budgeting process to assist with the preparation of clinical trial budgets. Working knowledge of FDA Code of Federal Regulations (CFR) and ICH Good Clinical Practice (GC) for clinical research.