Director of Clinical Operations Jobs in Daytona Beach, FL
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.
Research Director Center for Aerospace Resilient Systems
- Daytona Beach, FL
- 45+ days ago
- Daytona Beach, FL
- 45+ days ago
About Embry-Riddle Aeronautical University: As the largest and most comprehensive aviation and aerospace-focused university in the world, Embry-Riddle Aeronautical University (ERAU) is a unique...
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Salary for Director of Clinical Operations Jobs in Daytona Beach, FL
Required or preferred licenses and certifications for Director of Clinical Operations positions.
Highest Education Level
Director of Clinical Operationss in Daytona Beach, FL offer the following education backgroundQualifications / Skill Sets
The following top skills are often required or desired to land a Director of Clinical Operations position
- Mentoring
- Therapeutic
- Implementation
- Budgets
- ICH GCP
- Institutional Review Board
- Clinical Trial Management System
- Study Management
- Biomarkers
- ICH Guidelines
- Good Clinical Practice
- Lab Safety
- Cancer Research
- Drug Discovery
- Biostatistics
- Pharmacovigilance
- Computational Biology
- Field Sampling
- Medical Affairs
- Cancer Biology
- Scientific Research
- Drug Development
- Virology
- Site Management
- Microbiology
- Biology
- Immunology
- Neuroscience
- Clinical Trials
- Biotechnology
- Infectious Disease
- Clinical Operations
- Clinical Research
- Oncology
- FDA Regulations
- Medical Device Sales
- Research and Development
- Public Health
- Data Collection
- Standard Operating Procedures
- Data Management
- Engineering
- Health Care
- Affirmative Action
- Strategy Development
- Collections
- Military Background
- Investigation
- Presentation
- Data Analysis
- Documentation
- Collaboration
- Reporting
- Education Experience
- Regulations
- Policy Development
- Project Management
- Research Skills
- Problem Solving
- Staff Supervision
- Organization
- Scheduling
- Leadership
- Communication Skills
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