Provide clinical oversight in accordance with HHO core competencies and guidance for HHO operations, including, but not limited to, participant / case / project assignments, staff employment transactions, implementation of policies and procedures, staff training, etc.
Direct all aspects of the assigned US Medical Office Research program studies, including Medical Office Company Sponsored Studies (MACS) and Investigator Initiated and Sponsored Research (IISR) studies for multiple therapeutic areas and product programs. Manage Therapeutic Area (TA) and product level study budgets and communicate study activities to internal stakeholders.
Establishes and maintains policies, standards and programs for the provision of optimal, cost-effective nutrition care to patients/residents. This includes coordinating and directing all clinical activities and determining and implementing appropriate staffing levels.
This position is responsible for leading and managing the development, implementation, strategic day-to-day administration of managed care operations in a variety of clinical functions such as Utilization Management, Case Management and Disease Management.
Responsible and accountable for establishing and achieving departmental goals for each clinical trial by ensuring his/her FCSs have the knowledge, tools, and training to execute each clinical trial, by assisting his/her FCSs at their centers, and by interacting with internal and external customers, as needed, to attain the execution goals of the study.
This position is responsible for directing a team of clinical and non-clinical staff in quality management and quality improvement activities including HEDIS, QRS reporting, NCQA accreditation and regulatory compliance and submissions.
Responsible for supporting and driving FMS quality standards through meeting all ESRD regulatory requirements and the practice of Quality Assessment and Improvement (QAI), including use of FMS QAI tools.
Manager responsible for the overall assessment of compliance, quality control and/or standards defined for the execution of clinical trial(s); including managing CAPA, supporting process improvement initiatives and preparing/analyzing metrics.