Job Description

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 forms, drug dispensation records, and regulatory forms;
• Oversees subject enrollment to ensure that informed consent is properly obtained and documented
• Records adverse events and side effect data and confers with Investigators regarding the reporting of events to oversight agencies
• Documents findings and events in the Company’s research CTMS platform and in other binders and platforms as directed

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