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 requires experience with clinical research study execution, strong organizational skills, and the ability to thrive in a fast-paced environment.

Responsibilities

• Manage clinical study sites and documentation
• Manage vendors
• Develop clinical trial timelines and enrollment projections
• Develop protocols, informed consent forms, and training materials
• Review site regulatory documents
• Maintain relationships with investigators and vendors
• Participate in process improvement activities

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 Suite
• Ability to work in a team environment
• Ability to manage multiple tasks and shifting priorities
• High attention to detail and accuracy

Benefits

• No benefits