Director of Clinical Research

JOB SUMMARY The Director of Clinical Research is responsible for the development, implementation, and coordination of personnel supporting clinical trial operations for designated sites across Innovo’s site network. Directs, plans, and coordinates clinical research activities to ensure goals and objectives are accomplished within the prescribed timeframe and sponsor expectations. Oversees recruitment, management, and retention of research staff. Also the understanding that although this is a remote role, please be aware that there will be travel to the clinical research sites, up to 45%. RESPONSIBILITIES The Director of Clinical Research is responsible for developing, implementing, and coordinating a team of highly skilled professionals to ensure the successful execution of clinical trials. The focus will be on achieving goals and exceeding sponsor expectations while maintaining the highest standards of quality, compliance, and fiscal performance in clinical trials. In addition, this position will provide leadership and mentorship to your team and foster a collaborative and growth-oriented environment. Lead and motivate a team of clinical research professionals across designated sites of Innovo’s site network. Manage staff in accordance with the organization’s policies and applicable regulations. Includes planning, assigning, and directing work; appraising performance and guiding professional development; rewarding and disciplining employees; addressing employee relations issues and resolving problems. Approve actions on human resources matters, as applicable. Develop managers within the area of accountability to develop staff along career progression aligned with strategic departmental and corporate priorities. Oversees regional talent development. Evaluate workload, quality, and performance metrics through regular analysis of data. Initiate action plans to improve efficiency, quality, compliance, and fiscal performance. Ensures the Innovo site network meets the performance metrics required by the business and provides solutions to meet expectations if needed. Implement effective risk management strategies to proactively identify and address potential problems with operational performance, timeliness, and quality of research. Directs staffing and resource planning and allocation across clinical trial projects including staffing, training, quality assurance, and site evaluations. Directs regularly scheduled reporting to program executive leadership; reviews quality assurance reports generated by the data management core and develops plans with sites for corrective actions, as needed. Ability to travel to the sites. Performs related duties as required.