Senior Clinical Trial Associate (Sr. CTA)

Responsibilities

• Interact with Clinical staff, site staff, and vendors to support project-specific tasks and clinical trial management
• Manage study system access and deactivation
• Coordinate materials for internal and external meetings
• Distribute safety alerts and relevant documents
• Maintain study team and vendor contact information
• Assist in planning and executing study-specific meetings, including writing agendas and minutes
• Ensure completeness of documents in Trial Master Files (TMF) and ensure compliance with SOPs and ICH GCP Guidelines
• Develop and maintain study-related trackers to support Clinical Operations

Requirements

• Bachelor's degree in a relevant subject area or equivalent experience
• Minimum 2+ years in the biotech, pharmaceutical, or clinical trial management industry
• Competency in the drug development process and knowledge of ICH-GCP
• Strong interpersonal, organizational, and planning skills
• Proactive self-starter with the ability to execute tasks seamlessly
• Ability to travel up to 35%

Benefits

• Annual bonus opportunity
• Medical, dental, vision, life, and AD&D insurance
• 401(K) plan with match
• Stock options
• Flexible non-accrual paid time off
• Parental leave