The Department of Biostatistics in the School of Public Health (SOPH) at the University of Alabama at Birmingham (UAB), is inviting applications for the Director of the DATA coordinating and Collaborative Research Unit (DATA CRU, ), a team of specialized research professionals providing data coordinating center (DCC) operations for longitudinal cohort studies and randomized clinical trials. This position will be a key driver of the further development, management, and activities of the DATA CRU. This is a tenure earning appointment as an Associate Professor or Professor in the School of Public Health.

As the senior faculty member leading the DATA CRU, the Director will oversee a large staff responsible for day-to-day DCC operations and coordinate resources among multiple projects with specific Principal Investigators, staff leaders, and faculty co-investigators. The Director will work with multidisciplinary investigators on the development and conduct of new multicenter studies and trials, communicate data management needs and statistical concerns to statistician and non-statistician collaborators, and contribute to statistical analyses for presentation and publication. Importantly, the Director will guide the future direction of DCC operations to capitalize on existing areas of strengths (e.g., neurology, cardiology, maternal/fetal medicine, pediatrics) and to expand strategically into areas of growth (e.g., oncology) in the SOPH, UAB at large, and beyond, and advocate for resources needed to carry out those objectives.

Founded in , the UAB SOPH has grown to 84 full-time faculty and students (in the -24 academic year). The UAB SOPH is the only CEPH-accredited public health program in Alabama and both the school (18th) and department (13th) are ranked in the top 20 nationally by U.S. News & World Report. The SOPH is second only to the School of Medicine at UAB for extramural research funding among all 12 schools at UAB. In , the UAB SOPH had more than $42 million in grants and contracts and ranked 29th among all Schools of Public Health and 19th for all Public Schools of Public Health for NIH funding. UAB is a very high research activity (R1) university ranked 13th among public universities in NIH funding and 25th (top 5%) of all universities in NIH awards and an academic health center that discovers, teaches, and applies knowledge for the intellectual, cultural, social, and economic benefit of Birmingham, the state, and beyond. Spanning more than city blocks, UAB is the state of Alabamas largest single employer with some 25, employees and has an annual, state-wide economic impact exceeding $12.1 billion. Forbes named UAB Americas Best Large Employer for and best in-state employer in .

Responsibilities will include: · Lead a staff of over 40 clinical research specialists and coordinators, program managers and project directors, statisticians, and computer programmers, and be responsible for the organizations growth and changes to move the DATA CRU forward · Collaborate on the development and submission of multicenter and multinational funding applications for randomized clinical trials and cohort studies with a DCC component · Develop and oversee budgets for multicenter DCCs · Identify and plan statistical tasks, timelines, and resources with project teams and account for critical dependencies and resources to ensure that statistical work meets deadline commitments and quality standards · Oversee and participate with project teams in documentation management related to clinical trials including case report forms, electronic data capture, and data management validation plans and their deployment · Provide expert advice on the design of protocols, statistical analysis plans, and data management plans within grants and contracts. · Provide statistical advice on complex statistical problems and perform statistical analyses · Contribute to the definition and oversight of the setup, methodology, decision making, support, and implementation of DCCs · Contribute to the oversight and mentorship of junior faculty members, statisticians, data managers, and computer programmers · Participate in interdisciplinary meetings and videoconferences to provide consulting, interpretive, and analytical support · Evaluate compliance with current and relevant clinical and statistical regulatory requirements (e.g., GCP, ICH, CDISC, FDA, and other requirements) · Represent the Department of Biostatistics in the internal and external research communities in developing and conducting studies · Drive statistical thinking and knowledge across programs · Encourage new statistical methodologies and make recommendations, or capitalize on opportunities where new methodology or approaches could save costs and time

Applications will be accepted until the position is filled. To apply for this position please submit a CV and cover letter through the online portal at: | Applicants are asked to include with their online application: 1. A cover letter describing what they see as their future potential contribution with respect to establishing and leading a data coordinating center. 2. An up-to-date curriculum vitae detailing publications, coordinating experience, teaching, and funding history WittKieffer is assisting with this search. For questions regarding this position, contact

Required Qualifications PhD, ScD or DrPH in Biostatistics or related field with emphasis on applied statistical methodology 5 years of experience in clinical or biostatistical research A record of scholarship, teaching, and service to warrant appointment as a tenured or tenure-earning professor or associate professor at UAB

Preferred Qualifications Demonstrated leadership capabilities Experience leading clinical trials and multicenter studies Experience leading project teams Evidence of successful collaboration and communication with clinical researchers Experience with program management to ensure trial tasks are completed on time Experience as a faculty member in a biostatistics or equivalent department Experience with statistical analysis of biological data Experience from supervision of colleagues Experience with SAS, R, or other programming languages or packages Experience with clinical and statistical regulatory requirements (e.g., GCP, ICH, CDISC, FDA, and other requirements) Excellent written and oral communication and presentation skills