Clinical Research Coordinator | School of Medicine, Neurology

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/ **Unit:** School Of Medicine MBU **Department:** Neurology **Department** **Summary:** The Department of Neurology has a talented, robust team of faculty and staff members spanning nine divisions including representatives from every neurology subspecialty in adult and child neurology, plus award-winning educators, clinical and translational neuroscientists and master clinicians. **Duties & Responsibilities:** This position would serve as the clinical research coordinator for the Center for Inherited Myology Research. This center is responsible for developing disease modifying and other innovative therapies for individuals with muscular dystrophy. In this role, the incumbent works with a group that leads an international network aimed at achieving this objective. For all clinical research studies assigned, the Clinical Research Coordinator is responsible for coordinating clinical research activities in a compliant and efficient manner from study initiation to close out. Under the direction of the Principal Investigator (PI), collaborates 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. Core responsibilities are listed below along with other tasks and duties as assigned. Core Responsibilities: Research and Clinical Trial Coordination/Study Conduct (30%) - Independently coordinate study recruitment activities: pre-screening, screening - Access allowable data capture/retrieval systems and interact with a variety of health care delivery systems to identify potential study participants - Conduct and document the initial and ongoing informed consent process for research participants throughout study participation and follow up - Coordinate the enrollment of participants, coordinate and file randomization documents; notifying applicable individuals of registration/randomization (PI, participant, study team, pharmacist, etc.) - Support the PI and other study staff in following study participants through all study activities to ensure that the study is conducted in compliance with all requirements - Work with PI and program staff to ensure all required study close-out activities are complete. - For assigned studies, coordinate clinical research processes and documentation which may include: filing and office organization, creation of job aids, conducting protocol related training, research participant scheduling, ordering of study materials and supplies, and scheduling of meetings Regulatory and Compliance Requirements (25%) - Understand and adhere to all human subject protection and IRB regulations required for clinical research. - Understand duty to report obligations related to research conduct, and the appropriate university channels for reporting concerns - Participate in meetings with internal and sponsor appointed monitors to ensure accuracy of subject data and compliance with research protocol and regulatory requirements. - Coordinate auditing and monitoring activities for assigned studies. Data Management (25%) - Assist PI and study team members in the management of study data for new and ongoing clinical research studi…