MANAGER-CLINICAL RESEARCH COORDINATION

Manager-Clinical Research CoordinationThe University of Alabama at Birmingham (UAB), Department of Med - Cardiovascular Disease, is seeking a Manager-Clinical Research Coordination. General Responsibilities To manage all aspects of research program and clinical studies including education/teaching. To oversee and manage multiple clinical research protocols and the associated personnel. To design best practices for management of IP for drug, device, and biologic studies. To prepare study budgets. To manage research staff within area including all applicable human resources functions.Key Duties & Responsibilities Provides leadership and operational oversight for a complex clinical research program involving multiple clinical studies and research personnel. Serves as a key resource for faculty, sponsors, and research staff, ensuring studies are conducted in compliance with institutional, sponsor, federal, and regulatory requirements. In addition to managing study operations, this role is responsible for supervising and mentoring research staff, driving quality improvement initiatives, overseeing clinical trial management systems, and conducting quality assurance activities. The position offers an opportunity to influence research operations, develop best practices, and contribute to the growth and success of the CCTU. The ideal candidate will have significant experience managing clinical research operations, staff, and regulatory compliance in a complex academic medical center, healthcare, or research environment. Performs other duties as assigned. Annual Salary Range : $77,640 - $126,170Qualifications Bachelor's degree in a related field and eight (8) years of related experience required. Work experience may NOT substitute for education requirement. Certified Clinical Research Coordinator (CCRC) or Certified Clinical Research Professional (CCRP) certification strongly preferred. Preferences Degree in Clinical Research, Public Health, etc. Certified Clinical Research Coordinator (CCRC) or Certified Clinical Research Professional (CCRP) certification strongly preferred. Preferred Hard Skills: Clinical research operations management, Knowledge of FDA regulations, ICH-GCP guidelines, and human subject research protections. Experience managing multisite and/or industry-sponsored clinical trials. Experience with Clinical Trial Management Systems (CTMS), such as OnCore. Experience with Electronic Data Capture (EDC) systems Quality assurance, auditing, and regulatory compliance oversight. Research program development and process improvement. SOP development and implementation. Project management. Experience with institutional research systems such as IRAP and OnCore. Preferred Soft Skills: Leadership and staff development. Staff training and competency development. Coaching, mentoring, and training. Strategic thinking and problem-solving. Excellent organizational and prioritization skills. Strong written and verbal communication skills. Collaboration and relationship building with faculty, sponsors, and interdisciplinary teams. Conflict resolution and performance management. Ability to manage multiple competing priorities in a fast-paced environment.Primary Location: UniversityJob Category: Clinical ResearchOrganization: 311401000 Med - Cardiovascular DiseaseEmployee Status: Regular Shift : Day/1st Shift Work Arrangement (final schedule to be determined by the department/hiring manager) : Onsite