Responsible for leading a multi-year strategic program to build amgens clinical data repository and risk based monitoring solution and own the service after it is delivered. Programs vision includes developing a state-of-the-art solution in partnership with amgens strategic partners to deliver a platform that includes a patient data repository, operational data repository, clinical trial operational analytics & reporting, medical monitoring and support is capabilities required for enabling centralized monitoring/rbm risk based monitoring.
Manager, appeals & grievance will supervise the grievance and appeals nurse staff. The manager meets regularly with medical management staff with close interface with program medical directors in clarifying and resolving clinical grievance and appeal cases.
As a clinical supervisor of our hemodialysis team, the natural leader we select will provide direction, inspiration, and counseling to staff members, and coordinate all aspects of care, from admission to discharge. In addition, this individual will hire, train, lead a team, and ensure quality control and compliance with laws and regulations.
In this role, the selected candidate will be accountable for timely completion of patient care assessments and care plans by organizing meetings of the facility's Interdisciplinary Team to discuss patient care plans and to resolve patient problems.
If you value quality and excellence in care and developing a world class clinical team this may be the right opportunity for you. We specialize in providing integrative, preventive medicine programs for VIP clients.
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.
Primarily responsible for the implementation of Edwards Collaborative Practice programs at the direct facility level. Formulates plans in cooperation with the Director of Clinical and Economic Services and facility management for the implementation of evidence-based standards.
The Manager, Clinical and CMC Planning is responsible for supporting Clinical Trial/Project Teams by strategically developing and maintaining clinical study and CMC timelines, providing evaluations of potential risks and conflicts, supporting the team on proactively resolving potential deviations, and presenting clear timeline reports.
Develop detailed project plans to meet clinical objectives based on cross-functional input and analysis. Through collaboration and influence, gain core team buy-in and team ownership of the plan. Scope: Protocol writing, enrollment, monitoring, data cleaning and lock, biostats, safety, clinical submission deliverables, etc..