Responsible for creating appropriate protocol specific manufacturing and packaging work orders in concert with Third Party and IRT vendors, QA, clinical team partners etc. to ensure timely availability of clinical supplies.
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.
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.
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 the maintenance of clinical records and files to comply with Conditions of Participation (COPs), using measurements, as licensure, certification, and accreditation results.
In this role, you will managing the clinical study timelines, deliverables and risks, working with the client and Business Services to finalize the project budget and scope, serving as primary contact with client to ensure appropriate communication, managing project budget, and participate in internal and external meetings.
Ensures completion of new hiring orientation and training including mandatory in-services and ICD-9 code training when applicable; ensures documentation completed for annual in service training, and policy and procedure in service updates.
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 Senior Project Manager will lead the cross functional project teams including clinical operations, data management, biostatistics, medical writing and clinical QA, to ensure quality, on-time and within budget deliverables for primarily Phase II-IV clinical trials.
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.