Similar Jobs
See allClinical Trial Manager
Precision for Medicine
Europe
Oncology
MS Office
CTMS
Sr. Clinical Study Manager
Intuitive
US
Clinical Research
Data Analysis
Project Management
Manager of Clinical Trial Managers II
Abbvie
Global
People Management
Clinical Research
Strategic Thinking
Senior Manager/Associate Director Clinical Monitoring Strategy & Optimization
Oruka Therapeutics
US
Clinical Operations
ICH-GCP
Vendor Management
Clinical Research Associate - FSP - Remote
ICON
ICH-GCP
Regulatory Compliance
Communication
Position Summary:
- Manage all aspects of clinical trials from start-up through close-out.
- Ensure study timelines, costs, and quality metrics are met in compliance with regulations.
Primary Responsibilities:
- Oversee vendor/CRO selection and management, study contracting and budgeting.
- Lead protocol preparation, investigator selection, training, and monitoring.
- Hire, train, and oversee clinical trial staff; mentor junior staff.
Qualifications:
- Bachelor's degree in life sciences; 8+ years clinical research experience including 4+ years managing trials.
- Knowledge of FDA regulations, ICH-GCP, SOPs; strong analytical and organizational skills.
Natera
Natera is a global leader in cell-free DNA testing, dedicated to oncology, women’s health, and organ health. The team consists of highly dedicated professionals from world-class institutions who care deeply for their work and each other.