Clinical Project Manager for Multi-Site Trials
Advanced Resource Managers
Join our team as a Clinical Project Manager II, overseeing multi-site clinical trials from initiation to close-out. Lead project execution while ensuring compliance with regulatory standards and sponsor expectations. This role requires a clinical research professional with a BSc and over 5 years of experience, including a minimum of 3 years managing Phase I-III clinical trials. Your ability to manage timelines, budgets, and vendor relationships will be key. Experience in dermatology or rheumatology trials is a plus, setting you up for success in this dynamic environment. Key Responsibilities:
- Serve as the sponsor's main contact for updates
- Lead planning, activation, and deliverable management
- Supervise budgets, timelines, and resource utilization
- Ensure compliance with regulations and quality standards
- Monitor recruitment and implement risk strategies
- BSc in a clinical research-related discipline
- At least 5 years of industry experience
- 3+ years managing Phase I-III clinical trials
- Experience with multi-site studies is essential
- In-depth knowledge of GCP and regulatory affairs
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