Role OverviewThe Clinical Operations Manager is responsible for leading the planning, execution, oversight, and close-out of clinical studies that support the organization's research and development objectives.
What You Will Do
The Clinical Operations Manager provides operational leadership throughout the clinical trial lifecycle, including study startup, execution, monitoring oversight, risk management, vendor management, budget oversight, and inspection readiness.
Why It Might Be a Fit
Success in this role requires strong project management, collaboration, problem-solving, and communication skills in a dynamic and evolving environment.
Requirements
- Bachelor's degree in Life Sciences, Health Sciences, Nursing, Biomedical Engineering, Public Health, or related discipline
- Five or more years of experience managing clinical studies, clinical operations programs, or related research initiatives within the medical device, biotechnology, pharmaceutical, or CRO environment
- Working knowledge of applicable clinical research regulations and standards, including FDA regulations, ISO 14155, and ICH-GCP
- Experience managing external vendors, CROs, and study partners
- Demonstrated project management and operational leadership experience
Benefits
- Competitive salary
- Benefits package
- Opportunities for professional growth and development
]]>