Senior Director of Operations Position Available In Davidson, Tennessee

Clinical Site Sr Director – Lead Innovation in Clinical Research About the

Opportunity:

Join a premier clinical research organization with over 30 years of experience and a network of 32 locations across the U.S. Dedicated to advancing healthcare innovation through ethical, high-quality research practices, this organization offers a collaborative, mission-driven environment where excellence, integrity, and community are at the forefront. As a Clinical Site Sr Director, you will have the opportunity to drive operational excellence, build high-performing teams, and oversee the successful execution of clinical trials while helping shape the future of medical research.

Key Responsibilities:

Lead and oversee the daily business and clinical operations of the research site, ensuring efficiency, compliance, and performance against financial, operational, and quality targets. Manage site budgets, identify cost-saving opportunities, and ensure financial goals are consistently met or exceeded. Provide operational leadership across clinical trials, including study feasibility, patient recruitment, staffing, and regulatory compliance. Ensure site adherence to internal SOPs, GCP/ICH guidelines, and applicable regulatory requirements. Collaborate with senior leadership, site investigators, and external stakeholders to expand research capabilities and support business development efforts. Oversee recruitment, development, and retention of site staff, ensuring workload balance, performance management, and ongoing training needs are met. Identify potential risks to study execution and site performance, leading proactive efforts to mitigate issues and escalate when necessary. Drive patient recruitment initiatives and make real-time adjustments to ensure enrollment goals and financial projections are achieved. Foster a culture of collaboration, continuous improvement, and excellence, sharing best practices across sites to elevate organizational performance.

Desired Skills and Qualifications:

Bachelor’s degree preferred; equivalent experience may be considered in lieu of a degree. 5-10 years previous leadership roles within the Healthcare environment Minimum 5-10 years of clinical research industry experience. Minimum 5-10 years of proven management experience, leading clinical operations teams or managing research site functions. Expertise in project management with a strong ability to lead people, manage multiple priorities, and ensure project delivery within established timelines. In-depth understanding of clinical trial processes, regulatory standards, and quality management systems. Excellent interpersonal, communication, and presentation skills with the ability to foster positive relationships with internal teams, sponsors, CROs, and external vendors. Proficiency with MS Office applications and clinical trial management systems (e.g., Clinical Conductor CTMS). Strong financial acumen with experience managing site budgets and forecasting. Ability to travel up to 25% as needed for meetings, conferences, and site activities. Demonstrated professionalism, integrity, flexibility, and a proactive approach to problem-solving.

Residency Requirement:

Applicants must reside in one of the following states: Alabama (AL), Arizona (AZ), Florida (FL), Kansas (KS), Kentucky (KY), Louisiana (LA), Michigan (MI), Missouri (MO), Nevada (NV), Tennessee (TN), Utah (UT), or Virginia (VA).