Clinical Research Regulatory Specialist – Hybrid in Nashville TN

Discover Vanderbilt Health : With eight hospitals and over 180 clinics, we are the region’s largest comprehensive academic health system. Vanderbilt Health has a long tradition of providing world-class care to the people of the Mid-South, living out our mission of moving medicine forward through preeminent programs in patient care, education and research. Here you’ll find a spirit of collaboration and a supportive community where your expertise is valued, your knowledge expanded and your uniqueness celebrated. We are committed to fostering an environment where talented, compassionate people are united in bringing the most advanced care to our neighbors throughout the region. Organization: VICC- Clinical Trials 200 Job Summary: The Research Regulatory Analyst will act as a liaison to the IRB and assist with coordinating the approval processes and regulatory components of research protocols from study start-up to close-out, such that the integrity and quality of the clinical/translational research is maintained, and the research is conducted in accordance with all regulatory policies. . Preferred Skills & Experience Experience coordinating clinical research trials Experience obtaining informed consent from study participants Proficiency in Microsoft Excel and other Microsoft Office applications Experience with REDCap data management systems Clinical or translational research experience Hands-on involvement in all phases of clinical research trials IRB submission and regulatory compliance experience Strong ability to manage multiple priorities in a fast-paced environment Exceptional attention to detail and organizational skills Oncology research experience Key Responsibilities: Independently collects, reviews, organizes, assembles, and maintains regulatory documents/binders (paper and electronic) for assigned clinical trials, assuring the research information is collected and stored in a manner that is compliant with regulations/policies and good clinical practice. Independently prepares, reviews, and processes new IRB research proposals, amendments, continuing review applications, and adverse event reports according to institutional and departmental policies and federal regulations while maintaining timelines for studies from start-up to close-out. Proficient with OnCore, Veeva, and project management tools. With occasional guidance, initiates and performs quality control (QC) audits of regulatory documents from OnCore and Veeva. Generates QC Report summarizing the findings. Review pertinent regulations and guidance to develop proactive solutions to regulatory issues and challenges as evident by monitor/auditor follow-up letters. Assist with building relationships with internal/external stakeholders (i.e., monitors, auditors, and sponsors) by fostering a culture of respect and practicing active communication. Demonstrates knowledge and understanding of the Federal regulations and guidelines governing the protection of human subjects, e.g., FDA, OHRP, GCP/ICH, and HIPAA regulations. Supports team working relationships within assigned departments between all levels of personnel by fostering a culture of respect, communication, and ownership. The responsibilities listed are a general overview of the position, and additional duties may be assigned. Technical Capabilities: Communication (Intermediate): Clearly, effectively, and respectfully communicate with employees or customers, including external and internal stakeholders i.e., monitors, auditors, and sponsors. Problem Solving (Intermediate): Uses critical thinking and process improvement i.e., coaches and mentors’ development of problem statement, describes current state, identifies root causes, creates future state, coaches and mentors’ development of solutions and action plans with a sustainability plan. Applies appropriate tools to address issues. Project Coordination (Intermediate): Performs project tracking and reporting relative to task completion dates, dependency effects, problem anticipation, schedule conflicts, and assignment to appropriate staff for resolution. Assumes responsibility [as appropriate] for resolving issues and seeing work through to successful completion. Quality Assurance (Intermediate): Understands the goal of increasing organizational productivity and individual performance by making the products and services within your work assignments more efficient and more effective. Regulatory Compliance (Intermediate): Demonstrates knowledge of the appropriate rules and regulations and applies them in difficult, stressful, and complex situations. Able to interpret and explain rules and regulations that are ambiguous or unclear. Our Academic Enterprise is one of the nation’s longest serving and most prestigious academic medical centers. Through its historic bond with Vanderbilt University and integral role in the School of Medicine, Vanderbilt Health cultivates distinguished research and educational programs to advance a clinical enterprise that provides compassionate and personalized care and support for millions of patients and family members each year. World-leading academic departments and comprehensive centers of excellence pursue scientific discoveries and transformational educational and clinical advances across the entire spectrum of health and disease. Aligning with Vanderbilt Health’s Strategic Directions , the Office of Research provides shared research resources, administrative expertise and professional guidance to enable the trans-disciplinary environment and highly collaborative culture that advances discovery and training for all the research faculty, trainees, students and staff.  Core Accountabilities: Organizational Impact: Executes job responsibilities with the understanding of how output would affect and impact other areas related to own job area/team with occasional guidance. Problem Solving/ Complexity of work: Analyzes moderately complex