Director of Project Management Jobs in Vermont
In the biotechnology industry, a Director of Project Management plays a crucial role in overseeing and managing the planning, execution, and completion of various projects. These projects could range from biomedical research, product development, to clinical trials, among others. The Director ensures that projects are completed on time, within the allotted budget, and meet the set quality standards. They also liaise with different teams and stakeholders, manage risks, resolve issues, and establish project objectives and performance metrics. It's part of their responsibility to maintain a consistent line of communication with team members to ensure all are aligned with the project goals and expectations.
A Director of Project Management should have a strong background in science, especially in life sciences or bioengineering. They should possess excellent leadership, team management, and communication skills. They should be adept at strategic planning, problem-solving, and have a strong understanding of financial management. Proficiency in project management software tools and a good understanding of regulations and guidelines in biotechnology is also essential. Certifications such as PMP (Project Management Professional) or PgMP (Program Management Professional) would be beneficial. Prior to becoming a Director of Project Management, one could have roles such as Project Manager, Senior Project Manager, or Program Manager in the biotechnology or related fields.
**POSITION REQUIREMENTS** **:** + Strong knowledge of Good Clinical Practices (GCP), clinical trials management (including site monitoring), scientific methods, research design, regulatory compliance...
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Director of Project Managements in Vermont offer the following education backgroundQualifications / Skill Sets
The following top skills are often required or desired to land a Director of Project Management position
- Verbal Communication
- Forecasting
- Financial Management
- Budget Forecasting
- Implementation
- Budgets
- Institutional Review Board
- ICH GCP
- Study Management
- Clinical Monitoring
- Biomarkers
- Clinical Trial Management System
- Cancer Research
- Clinical Data Management
- Gene Therapy
- Good Clinical Practice
- ICH Guidelines
- Medical Affairs
- Biostatistics
- Drug Discovery
- Scientific Research
- Biology
- Drug Development
- Pharmacovigilance
- Immunology
- Medical Writing
- Stem Cells
- Biotechnology
- Clinical Trials
- Hematology
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- FDA Regulations
- Research and Development
- Data Collection
- Standard Operating Procedures
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- Health Care
- Strategy Development
- Collections
- Investigation
- Education Experience
- Interpersonal Skills
- Quality Assurance
- Collaboration
- Documentation
- Reporting
- Regulations
- Multitasking
- Microsoft Office
- Project Management
- Problem Solving
- Research Skills
- Microsoft Excel
- Staff Supervision
- Organization
- Scheduling
- Leadership
- Communication Skills
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