Clinical Research Coordinator C (Department of Neurology)

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Posted Job Title

Clinical Research Coordinator C (Department of Neurology)

Job Profile Title

Clinical Research Coordinator C

Job Description Summary

Clinical Research Coordinator C (CRC C) will be responsible for the coordination of multiple early phase, industry-sponsored and investigator-initiated clinical trials of nucleic acid-based therapies conducted in the TCE for NeuroGeneRx through their entire lifecycle (startup, conduct and closeout).

Job Description

Job Responsibilities

• Conducts and manages multiple clinical trials. Responsibilities include adherence to IRB protocols; consenting of study subjects, screening, recruiting and enrolling subjects; coordinating clinical treatment, study visits and follow-up care; administering diagnostic assessments; monitoring study charts; reporting adverse events.
• Responsible for the oversight, management and tracking of protocol execution from startup to completion. This includes but is not limited to preparing and processing regulatory documents to all regulatory committees; completion of initial and amendment IRB submissions for review; organizing, maintaining, and assuring the accuracy of all trial-specific documentation, including regulatory files, correspondence, source documentation, and research charts.
• Assists with clinical trial proposal process by generating internal (with Business Office) and external study budgets; collecting required clinical trial documentation to support contract negotiations between the sponsor and CTCU.
• Reviews internal budgets and monitor monthly clinical expenses including hospital services, subject payments and payroll. Submit invoices to sponsor per contract terms.
• Other duties and responsibilities as assigned.

Hiring range minimum for this position is $60,813.

Salary offers are made based on the candidate’s qualifications, experience, skills, and education as they directly relate to the requirements of the position