At least 2 years of experience in clinical research, clinical data management, or a comparable role
Bachelors degree in a related field or equivalent education and experience.
Intermediate to advanced proficiency with Microsoft Excel and Word.
Ability to utilize electronic medical databases and electronic health record systems, including experience with EPIC.
Strong understanding of Good Clinical Practice (GCP) principles and completion of GCP training.
Knowledge of federal regulations related to HIPAA and IRB requirements as they apply to clinical research.
Eligibility to work in a remote or hybrid capacity in approved states, as defined by organizational policy.