In this role, the selected candidate will support the goals of the Gen Med organization by initiating, monitoring, and closing out clinical study sites following GCP and ICH guidelines as well as Novartis SOPs and ensuring that study milestones are met.
The coordinator uses advanced nursing processes in decision-making, patient assessment, data analysis, development and implementation of methods and systems to improve the overall quality and efficiency of patient care for the designated department and population served.
In this role, you will organize and plans work with input from the patient/family with specific outcomes and demonstrated use Organizes work and delegates and supervises others (RN's, LPNs, Care Partners, Unit Secretaries, etc) in carrying out assignments of sound clinical judgment and resources.
In this role, you will demonstrate teamwork, flexibility and creative problem-solving skills when dealing with others including those culturally diverse, departmental staff, physicians, patients, or families.
This position will be responsible for the clinical management of research within the company to include coordination of all human subjects research/IRB, participation in initial and ongoing site visits and audits, management of multiple protocols involving patient screening, enrollment, treatment and education as well as coordination of patient care to adhere to timelines of clinical trials.