In this role, you will develop, implement and collaborate on training for company operating procedures, GCPs, protocols, database, compliance, device accountability, adverse event reporting, study investigation protocols, amendments, regulatory documentation requirements, process improvement as well as training and proctoring new employees on trial and study related activities.
In this role, you will be responsible and accountable for the deliverables of several clinical studies as part of a therapeutic program product strategy to support the expanding product portfolio for the business.
In this role, you will be 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.
The Clinical Program Manager is responsible for identifying, managing and tracking clinical, quality, correct coding, documentation and data submission projects that advance the objectives of Health Nets strategic goals.
In this role, you will participate in student program, as assigned, and provides a positive learning environment for students with appropriate supervision, development of learning objectives and completion of student evaluations.
In this role, the selected candidate will be responsible for responsible for implementation of FMS staffing, and medical supply models, to provide quality patient care, and makes recommendations to Area Manager.
In this role, you will provide internal communication of important clinical data and events. Functions as a reliable, trusted resource of accurate, up-to-date project knowledge as requested by key stakeholders.
In this role, you will be responsible to develops and maintains effective relationships through effective and timely communication. Responsible for implementing appropriate training according to fms policy, including training to ensure ongoing compliance with all fms risk management initiatives.