Director of Clinical Operations Jobs in Colorado
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.
Institutes policies that are compliant with ICH/GCP regulations and guidelines, as well as institutional policies and procedures....
Senior Clinical Research Project Coordinator - Denver
- Denver, CO
- 90+ days ago
- Denver, CO
- 90+ days ago
Medpace is a leading CRO for Biotech companies and we are currently seeking a full-time, office-based Project Coordinator to join our Clinical Trial Management team....
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Salary for Director of Clinical Operations Jobs in Colorado
Required or preferred licenses and certifications for Director of Clinical Operations positions.
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Director of Clinical Operationss in Colorado offer the following education backgroundQualifications / Skill Sets
The following top skills are often required or desired to land a Director of Clinical Operations position
- Implementation
- Budgets
- Institutional Review Board
- ICH GCP
- Clinical Trial Management System
- Study Management
- Biomarkers
- Good Clinical Practice
- ICH Guidelines
- Lab Safety
- Molecular Biology
- Drug Discovery
- Biostatistics
- Computational Biology
- Field Sampling
- Mass Spectrometry
- Medical Affairs
- Method Development
- Drug Development
- Biology
- Scientific Research
- Biochemistry
- Pharmacovigilance
- Stem Cells
- Nuclear Magnetic Resonance
- Immunology
- Gel Electrophoresis
- Biotechnology
- Clinical Trials
- Neuroscience
- Infectious Disease
- Clinical Research
- Clinical Operations
- Oncology
- FDA Regulations
- Research and Development
- Data Collection
- Standard Operating Procedures
- Data Management
- Health Care
- Engineering
- Affirmative Action
- Strategy Development
- Collections
- Military Background
- Investigation
- Written Communication
- Auditing
- Presentation
- Documentation
- Collaboration
- Reporting
- Education Experience
- Bachelor's Degree
- Regulations
- Project Management
- Problem Solving
- Microsoft Excel
- Staff Supervision
- Organization
- Research Skills
- Scheduling
- Leadership
- Communication Skills
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