Primary responsibilities include patient enrollment, screening, monitoring of research participants, and reporting to the clinical research sponsor. The Research Coordinator II will be responsible for ensuring accurate data collection, documentation, organization among a variety of TCH/BCM departments and safety of study volunteers.
This position will be working directly with physicians and investigators to follow up on study patients. Must have a working knowledge of FDA Good Clinical Practices, and the ability to read, analyze, and interpret information.
Applicants must be willing to work in a fast pace setting, comfortable working in a team environment, and possess excellent communication skills.
Open to candidates eligible for TN visa status.
