We are looking to add a full time onsite Clinical Research Coordinator to a growing research site.

Qualified candidates will have a minimum of 1 year of experience working on Sponsor funded studies and must be able to perform phlebotomy.

Responsibilities

• Performs study subject visits, Screening and recruiting subjects; Dosing and administering study drugs and/or implementing study methodologies
• Collecting, labeling, storing, and shipping specimens collected from subjects in connection with a clinical research trial
• Entering patient and research data in systems designated by the Company
• Maintaining patient charts and resolving research queries.
• Monitors study activities to ensure compliance with study protocols and with applicable federal, state, and local regulatory and Site requirements and policies;
• Maintains required records of study activity including case report form...