Prepare and actively participate as operational lead in internal project review meetings. Depending on size and scope of project, this job duty may be performed in collaboration with a Project Director.
Responsible for assembling project plans and teamwork assignments, directing and monitoring work efforts on a daily basis, identifying resource needs, performing quality review; and escalating functional, quality, timeline issues appropriately.
Work closely with Principal Investigators and study teams; participate in study-related conferences, as necessary; participate in development of strategic plans for new projects and facilities, serve in an advisory capacity on best practices for database development and maintenance.
The Clinical Program Manager will play a critical role in partnering, establishing and maintaining a high performing function that will be equipped to deliver the clinical aspects of the Client's portfolio.
Promotes a positive and professional image for pharmacy by advocating and demonstrating exemplary teamwork and leadership; participates and acts as the inter and intra department liaison in collaborations with nursing, ancillary department directors and medical staff.
This individual will also be responsible for daily monitoring and management of the supply chain for company sponsored clinical studies as well as relevant investigator initiated studies, including monitoring supply levels using IXRS systems.
Monitor team member ICSR quality and compliance, with an emphasis on SUSARs accuracy, completeness (e.g. case narratives, coding activities, AOSE, etc.) to maintain regulatory compliance and strong partnerships with stakeholders (GCO).