Job Description

The Clinical Trial Manager is responsible for overseeing and managing all clinical operational activities at the trial and site level, ensuring studies meet timelines and maintain high quality standards. This role involves collaboration with research staff, investigators, and vendors in a fast-paced environment.

Responsibilities

• Manage clinical study sites and documentation
• Manage vendors and complete project management tasks
• Develop clinical trial timelines and instructional materials
• Participate in process improvement and SOP development
• Conduct study start-up activities
• Review site regulatory documents
• Maintain relationships with investigators and vendors

Requirements

• Bachelor’s degree in science or health related field
• 5+ years of relevant experience
• Knowledge of ICH Guidelines, US FDA, and European clinical trial requirements
• Excellent written and oral communication skills
• Proficiency in Microsoft Office tools
• Ability to work in a team environment
• Ability to manage multiple tasks and shifting priorities
• High attention to detail and accuracy

Benefits

• No benefits