Director of Clinical Operations Jobs in Connecticut
A Director of Clinical Operations in the biotechnology industry oversees the planning, implementation, and management of clinical trials and research. They are involved in the development and execution of clinical strategies, and work collaboratively with professionals in regulatory affairs, drug safety, data management, and project management. Their work is crucial for ensuring adherence to protocols, regulatory requirements, and ethical standards, as well as achieving the company's clinical objectives. They are also responsible for managing teams, allocating resources, and overseeing the budgeting process.
The Director of Clinical Operations should ideally hold a degree in life sciences or a related field, with advanced degrees often preferred. Certifications in clinical research such as Certified Clinical Research Professional (CCRP) can be beneficial. They should have extensive knowledge of clinical trial management and regulatory compliance, coupled with exceptional leadership, strategic planning, and problem-solving skills. Prior to this role, an individual might hold positions such as Clinical Project Manager, Clinical Trials Manager, or Clinical Research Associate.
If you are passionate about clinical research and eager to contribute to innovative studies, we encourage you to apply! 9869634...
The Center for Policing Equity-Yale Lab is seeking an Executive Director -Research Scholar with a passion for executing high-quality quantitative social science to lead the growing lab. The...
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Salary for Director of Clinical Operations Jobs in Connecticut
Required or preferred licenses and certifications for Director of Clinical Operations positions.
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Director of Clinical Operationss in Connecticut offer the following education backgroundQualifications / Skill Sets
The following top skills are often required or desired to land a Director of Clinical Operations position
- Finance
- Spreadsheets
- Forecasting
- Financial Management
- Budget Forecasting
- Implementation
- Budgets
- Institutional Review Board
- ICH GCP
- Study Management
- Clinical Monitoring
- Clinical Trial Management System
- Biomarkers
- Cancer Research
- Clinical Data Management
- ICH Guidelines
- Good Clinical Practice
- Medical Affairs
- Biostatistics
- Drug Discovery
- Scientific Research
- Drug Development
- Biology
- Pharmacovigilance
- Immunology
- Medical Writing
- Stem Cells
- Biotechnology
- Clinical Trials
- Clinical Research
- Clinical Operations
- Oncology
- FDA Regulations
- Research and Development
- Public Health
- Standard Operating Procedures
- Masters In Education
- Data Management
- Engineering
- Strategy Development
- Military Background
- Investigation
- Interpersonal Skills
- Quality Assurance
- Collaboration
- Documentation
- Reporting
- Regulations
- Multitasking
- Microsoft Office
- Project Management
- Problem Solving
- Research Skills
- Staff Supervision
- Organization
- Scheduling
- Computer Skills
- Leadership
- Communication Skills
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