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Baptist Memorial Health Care Corporation is seeking a Program Manager to lead the REFLEX Precision Oncology Initiative, coordinating clinical operations, pathology, informatics, data science, and administration to expand timely biomarker testing and access to precision oncology care.
You will develop project plans, track milestones, prepare performance metrics, and manage grant deliverables while ensuring regulatory compliance and stakeholder engagement across multiple sites.
Overview
The Program Manager provides operational leadership and coordination for the REFLEX Precision Oncology Initiative, a multi-disciplinary implementation science program focused on expanding timely biomarker testing, supporting precision oncology care, and improving clinical trial access across Baptist Memorial Health Care. The Program Manager partners with clinical, research, pathology, informatics, data science, and administrative leaders to oversee program implementation, regulatory compliance, grant deliverables, performance measurement, and stakeholder engagement.
Minimum Education
Bachelor's degree in Healthcare Administration, Public Health, Biological Sciences, Clinical Research, Business Administration, or a related field.
Minimum Experience
Minimum of 3-5 years of experience in healthcare program management, clinical research, oncology operations, quality improvement, implementation science, or a related healthcare setting. Demonstrated experience coordinating multidisciplinary teams, managing complex multi-site initiatives, developing project plans, monitoring performance outcomes, and supporting regulatory or grant-funded research requirements.
Minimum Licensure, Registration, Certification
None required.
Desired Education
Advanced degree in healthcare administration, public health, clinical research, implementation science, business administration, health sciences, or a related field.
Desired Experience
Experience with grant-funded, multi-site healthcare or research programs, including milestone tracking, budget monitoring, sponsor/Foundation reporting, and site activation activities. Experience supporting clinical research and regulatory activities, including IRB submissions, amendments, clinicaltrials.gov updates, surveys, and study documentation. Experience in oncology, precision medicine, implementation science, or population health initiatives.
Desired Licensure, Registration, Certification
Project Management Professional (PMP), Certified Clinical Research Professional (CCRP), or similar certification.