
Director, Project Management – Oncology
Posted Aug 14

Posted Aug 14
This is a fully remote position, open to applicants in United States.
• Formulate partnership strategies for clinical trials and associated programs.
• Offer oversight and strategic insight in the planning, coordination, and execution of designated clinical study projects.
• Lead, manage, and ensure collaboration among Project Directors and Project Managers in global project and portfolio planning, implementation, and governance.
• Provide leadership and supervision on clinical programs.
• Act as the primary escalation contact for study sponsors beyond project management.
• Enhance the profitability of the Project Management organization in line with budgetary targets.
• Evaluate and manage resource allocations to achieve cost, time, and quality objectives.
• Select, train, mentor, and oversee Project Directors and Project Managers.
• Deliver technical support and guidance regarding scope, risks, resources, goals, and deliverables.
• Recognize and escalate issues affecting project scope, resources, schedule, or budget.
• Guarantee compliance with quality standards, SOPs, project plans, and regulatory requirements.
• Engage in business development, proposal submissions, budgeting, bid defense preparations, and participation.
• Manage interdependencies between projects and programs to meet milestones and deliverables.
• Assess projects and implement modifications, including recovering at-risk projects, re-scoping, postponing, or canceling as necessary.
• Measure and report on KPIs while leading continuous improvement initiatives.
• Oversee staff workload and make adjustments as required.
• Provide continuous feedback, development opportunities, coaching, and conduct annual performance evaluations.
• Bachelor’s degree or an equivalent combination of education and experience in a science or health-related field.
• At least 10 years of experience in clinical research, demonstrating extensive project management and line management expertise, or proven competencies relevant to the position.
• Comprehensive understanding of GCP/ICH guidelines and the clinical development process.
• Proficient with Microsoft Office Products (Outlook, Word, Excel, PowerPoint) and Microsoft Project.
• Exceptional communication and interpersonal abilities for effective collaboration.
• Strong organizational skills, meticulous attention to detail, and a customer service-oriented approach.
• Willingness to travel domestically and internationally, including overnight stays.
• Working knowledge of project management techniques and tools.
• Direct experience in a global, cross-functional project management setting.
• Proven experience in people management.
• Demonstrated expertise in strategic planning, risk management, and change management.
• Strong analytical capabilities and business insight.
• Professional presence with the ability to deliver complex presentations to senior management.
• Established leadership record and effective interpersonal skills.
• Proficient in project management software.
• Extensive proven experience in pharmaceutical and/or device research.
• Discretionary annual bonus.
• Health insurance.
• Retirement savings benefits.
• Life insurance.
• Disability benefits.
• Parental leave.
• Paid time off for sick leave and vacation.
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