Clinical Project Manager for Multi-Site Trials

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

Requirements:

• 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

Bring your expertise in clinical trials and leadership skills to drive successful outcomes in our projects. #J-18808-Ljbffr