Clinical Science Program Specialist

Job Summary

Managing multiple clinical testing and lab services projects remotely, the contract Clinical Science Program Specialist will coordinate project timelines, oversee sample process flow, and serve as the primary contact for Pharma customers.

Key responsibilities

• Manage clinical testing and lab services projects from initiation through contract completion under the supervision of the Program Manager
• Coordinate project timelines, develop project plans, and track progress while identifying delays or bottlenecks
• Interface with external resources, organize meeting activities, and communicate project reports and clinical study data to clients

Required qualifications

• Minimum of 2 years of project management or clinical trial coordination experience in a regulated environment
• Bachelor's degree required; Life Sciences preferred
• Exposure to clinical studies and projects requiring rapid milestone achievement
• Preferred experience in standard project management processes and clinical trial management
• Knowledge of diagnostic and pharmaceutical industry practices is a plus