At least 1 year of clinical research experience, with a strong understanding of clinical trial terminology and processes.
Experience in clinical research, data-focused roles, or clinic-based work that demonstrates familiarity with clinical workflows and trial operations.
Ability to perform detailed chart reviews to identify eligible patients and extract relevant clinical information.
Proficiency in pre-screening patients for clinical trials using established eligibility criteria.
Hands-on experience supporting clinical trials, including patient interaction and coordination activities.
Strong data entry skills with a high level of accuracy and attention to detail.
Experience in data management within a clinical or research environment.
Experience using electronic data capture (EDC) systems, with the ability to learn and work within multiple platforms.
Ability to work effectively within EPIC or similar electronic medical record systems for chart review and documentation.
Comfort working in a clinical environment and engaging directly with patients participating in research studies.