In this role, you will audit operations, including laboratory procedures, to ensure compliance with applicable regulations; provide leadership in identifying and implementing corrective actions/processes. Monitor Institutional Review Board submissions, and respond to requests and questions.
In this role, the successful candidate will be responsible for the coordination, administration and regulatory compliance of clinical trial documentation and investigational product traceability for the conduct of clinical trials during product research and development of ophthalmic medical device.
In this role, the selected candidate will ensure compliance with research protocols, and review and audit case report forms for completion and accuracy with source documents. Prepare regulatory submissions, and ensure institutional Review Board renewals are completed.
In this role, you will be responsible for identifying opportunities to improve patient care services; assisting clinic management to identify and develop operational needs for the clinic and to improve patient care services; and they may provide direct patient care.
The clinical coordinator is responsible for the delivery of safe, quality care of dialysis treatments by assisting the clinical manager with oversight of the centers operations and by providing direct patient care.
In this role, you will provide assistance in planning, coordinating, and delivering patient care for patients with liver disease using the nursing process, ensuring compliance with physician orders and established policies and procedures.