Clinical Research Coordinator, School of Medicine / Neurology, Neuroimmunology & Multiple Sclerosis

Virginia Commonwealth University (VCU) School of Medicine is a premier academic medical center located in the heart of Richmond. Accounting for almost half of VCU's sponsored research, the School of Medicine is internationally recognized for patient care and education. All full-time university staff are eligible for our generous benefits package that includes choices for health, vision, and dental coverage, life-insurance, short and long-term disability coverage, retirement planning, tax-deferred annuity and cash match programs, flexible spending accounts, tuition benefits, significant paid-time off, 12 paid holidays, and more. Explore our benefits further here: https://hr.vcu.edu/current-employees/benefits/university-and-academic-professional-benefits/

Summary

The Department of Neurology Neuroimmunology & Multiple Sclerosis (MS) Program is seeking to hire a Clinical Research Coordinator to support our active and growing research program. The Neuroimmunology & MS program is engaged in clinical research related to understanding environmental & modifiable risk factors that impact MS disease course, studies to validate innovative and new clinical outcome measures, and therapeutic clinical trials.

For all clinical research studies assigned, the Clinical Research Coordinator (CRC) is responsible for coordinating clinical research studies in a compliant and efficient manner. Under the direction of the Principal Investigator (PI), the CRC will collaborate with all members of the clinical research team to ensure all federal, state, university, and protocol requirements are followed, institutional research objectives are met, and that ethical obligations are kept.

Duties and Responsibilities

• Management of all duties required for clinical research studies from initiation to close-out.
• Conduct of clinical research activities as authorized by the Principal Investigator's documented Delegation of Authority and Training Logs.
• On-call coverage for research projects as needed
• Collaboration with department administrative staff and the School of Medicine Office of Research Administration, coordination of the initiation processes for Movement Disorders research projects and other clinical research projects in the Department of Neurology;
• Maintenance of current CITI credentials for Human Subjects Protections, Good Clinical Practice (GCP), Clinical Research Coordinator, plus additional sponsor GCP certifications as required.
• Understanding and adherence to all IRB requirements, Human Subjects protection regulations, and all aspects of IRB approved protocols.
• Conducting all assigned activities in compliance with national, local, & institutional guidelines, according to all HIPAA, GCP, and other applicable requirements.
• Study activities including coordinating new study activation requirements, screening/enrolling participants, regulatory and compliance requirements, maintaining appropriate study documentation/records, and managing study data.