Job Summary The Director of the Clinical Trials Program provides leadership, strategic planning, and operational oversight for the research facility. The director balances clinical excellence, regulatory compliance, and portfolio expansion. This position is responsible for cultivating multi-site partnerships, establishing a rigorous safety culture, and driving methodological and statistical excellence across all clinical and translational research initiatives. Core Job Responsibilities Strategic Leadership, Portfolio Growth & Research Design • The director drives the strategic expansion of the Clinical Trials Program by targeting public and private research grants supporting operational and project funds. • To broaden research offerings, the director scales investigator-initiated trials, builds multi-site grant initiatives, and serves as the core liaison between healthcare providers, institutional investors, pharmaceutical companies, academic partners, and sponsors. • Methodologically, the director researches design to optimize research proposals. • The director will lend assistance with research data analysis plans, sample size calculations, power analyses, and predictive modeling, while championing high-impact research dissemination through the review of statistical findings and manuscripts for peer-reviewed journals. Operations, Compliance & Risk Management • Ensures safety and operational compliance and patient and data safety. • Maintains open communication with the Institutional Review Board, manages conflicts of interest, and cooperates with the legal office regarding institutional compliance with regulations for patient privacy and safety. • Oversees bio-statistical standards such as data integrity and reproducibility, in alignment with regulatory guidelines, and ensures access to incident reporting. Financial Oversight, Infrastructure & Personnel • Directs comprehensive budget management systems encompassing revenue funding, expense distributions, and grant tracking, while driving long-term financial longevity via integrated billing frameworks and capital forecasting. • Defines precise internal roles and structural divisions of labor, mandating safety training courses, conducting operational evaluations, and overseeing continuous staff training in research methodologies and analytical software. • Performs other duties as required. Education/Experience Requirements REQUIRED: • PhD, MD, or related terminal degree in a life science, biostatistics, public health, or a related field • 8 years of leadership experience • Documented published peer-reviewed research. • Demonstrate expertise in quantitative and qualitative research methodologies, epidemiological principles, quality assurance protocols, and advanced statistical analysis. • Demonstrate financial acumen in budget management, grant tracking, and business intelligence tools, paired with an expert working knowledge of Institutional Review Board operations, and patient safety. • Highly proficient with MS Office. PREFERRED: • Proficiency in industry-standard analytical software such as SAS, SPSS, R, or Stata. Licensure/Certification Requirements Disclaimer Qualified applicants will receive consideration for employment without regard to their age, race, religion, national origin, ethnicity, age, gender (including pregnancy, childbirth, et al), sexual orientation, gender identity or expression, protected veteran status, or disability. Successful candidates might be required to undergo a background verification with an external vendor. Job Details Req Id 99264 Department RESEARCH AND SCHOLARLY ACT Shift Days Shift Hours Worked 8.00 FTE 1 Work Schedule SALARIED MANAGEMENT Employee Status A1 - Full-Time Union Non-Union Pay Range $120,000 - $192,000 annually