
Project Director
Posted 2 days ago

Posted 2 days ago
This is a fully remote position, open to applicants in Romania, +6 more countries.
• Act as the main point of contact for clients and engage in proposal activities and client presentations.
• Supervise all facets of clinical research trials and designated portfolios.
• Guide project managers through the processes of project establishment, planning, initiation, procurement, execution, and closure.
• Oversee study budgets, scope, change orders, and overall financial health.
• Manage project profitability, billable hours, billing, and forecasting.
• Create or supervise detailed project plans, timelines, risk management strategies, and mitigation efforts.
• Ensure quality management, eTMF inspection readiness, and implementation of corrective/preventive actions.
• Establish tracking metrics to monitor trial and team progress.
• Prepare project status updates, KPI reports, and solutions for clients and senior management.
• Facilitate internal and client meetings, advancing study-level strategies.
• Oversee cross-functional project teams and the execution of trials.
• Communicate issues related to protocols and studies, implementing necessary actions accordingly.
• Conduct formal presentations, including bid defenses.
• Ensure compliance and training specific to studies.
• Assist with business development and marketing efforts, including travel for bid defenses.
• Mentor associate, project, and senior project managers.
• Contribute to departmental updates and the development of company SOPs.
• Provide continuous feedback and conduct annual performance reviews for team members.
• Identify performance issues at the project level and ensure corrective actions are taken.
• Execute assigned responsibilities and administrative tasks, including training and time reporting.
• Degree or an equivalent combination of education and experience in a science or health-related field for EU candidates; advanced degree preferred.
• At least 8 years of clinical research experience or proven competencies related to the position.
• Minimum of 5 years of direct project management experience.
• High proficiency in Microsoft Office Products (Outlook, Word, Excel, PowerPoint), Microsoft Project, eTMF, EDC, and CTMS.
• Exceptional communication and interpersonal skills.
• Strong organizational skills and meticulous attention to detail.
• Orientation towards customer service.
• Experience managing highly complex and global studies or a portfolio of studies.
• Mastery of ICH-GCP guidelines and relevant Precision SOPs.
• Excellent understanding of project management techniques and tools.
• Extensive experience in cross-functional project management settings.
• Strong grasp of cross-functional management principles.
• Proven expertise in project planning, risk management, and change management.
• Highly experienced in pharmaceutical and/or device research.
• Demonstrated excellence in time management, negotiation, critical thinking, decision-making, analytical skills, interpersonal skills, presentation abilities, and both verbal and written communication skills.
• Expert knowledge of project management software.
• Well-developed skills in customer orientation, influence, negotiation, and conflict management.
• Ability to work and plan independently as well as in a team setting.
• Willingness to travel domestically and internationally, including overnight stays.
• Supportive and collaborative work environment.
• Emphasis on work-life balance.
• Opportunities for team development.
• Recognition and appreciation for employee contributions.
• Commitment to equal opportunity employment.
• Provision of reasonable accommodations during the application process.
Alzheimer's Association®
The College Board
The College Board
Cargill
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