The Department of OBGYN is seeking to hire a full time Clinical Research Coordinator to contribute to the overall operational management of clinical research / trial / study activities from design, set up, conduct, through closeout. In this role you will:

• Have responsibility for the implementation of research activities for one or more studies. 
• Recognizes and performs necessary tasks to manage projects and prioritizes work to meet necessary deadlines. 
• Be responsible for planning and organizing necessary tasks to ensure adherence to the study protocol and applicable regulations, such as institutional policy and procedures, FDA Code of Federal Regulations (CFR), and ICH Good Clinical Practice (GCP). 
• Collaborates with the Principal Investigator (PI), ancillary departments, central research infrastructure teams, sponsors, institutions, and other entities as needed to support the administration of all aspects of studies, including, but not limited to, compliant conduct, financial management, and adequate personnel support.
• Other duties as necessary.