In this role, the selected candidate will provide oversight for appropriate and compliant clinical episodic reimbursement; participate in the recruitment, interviewing, selection, and orientation of team members.
In this role, you will be responsible for the maintenance of clinical records and files to comply with Conditions of Participation (COPs), using measurements, as licensure, certification, and accreditation results.
Manage and lead the day-to-day operations of assigned studies to ensure completion per established project team goals and objectives in compliance with applicable GCP/ICH guidelines and other regulatory requirements.
Collaborates with internal resources to ensure maintains current understanding of us import/export regulations, reviews upcoming or potential regulation changes and proposals, and supports awareness of these changes across applicable functions within pfizer and third parties.
In this role, you will be responsible for supporting and driving quality standards through meeting all ESRD regulatory requirements and the practice of Quality Assessment and Improvement (QAI), including use of QAI tools.
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.