非公開
• Project Manager (PM) is responsible for the overall coordination and management of clinical trials from start up through closeout activities.
• Directs the technical, financial and operational aspects of the projects -- thus securing the successful completion of clinical trials.
• Works with functional area leads to identify and evaluate fundamental project requirements, interpret data on complex issues, is responsible for contingency planning and implementation of rescue strategy where needed and ensure solutions are implemented.
• Works to ensure that all project deliverables meet the customer’s time/quality/cost expectations
• The PM, with support from the Project Management Directors, working in collaboration with other functional area leads, is accountable for ensuring that all project deliverables meet the customer/contract expectations.
【RESPONSIBILITIES】
Tasks may include but are not limited to:
• Lead core project team members and facilitate their ability to lead extended/complete project team
• Lead cross unit coordination both internal and external, inclusive of sub-contractors
• Define and manage project resource needs in conjunction with functional heads and establish contingency plans for key resources
• Ensure successful design, implementation, tracking and revision of project plans for assigned projects
• Promote effective teamwork among project team members; resolve conflicts as needed
• Ensure appropriate communication on project-related matters with the PM Management
• Meet financial performance targets for the assigned clinical projects
• Ensure project deliverables are met according to both the company and client expectations
• Initiate improvements to enhance the efficiency and the quality of the work performed on assigned projects
• Act as key client contact for assigned projects
• Establish excellent working relationships with client project teams to ensure client satisfaction and operational excellence
• Ensure that all staff allocated to assigned projects are trained on the study protocol and all other study related processes, adhere to professional standards and to SOPs as well as current Good Clinical Practice (GCP) and applicable local regulations
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