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 projects from initiation through contract completion, ensuring timely delivery and effective communication with stakeholders
• Coordinate project plans and track progress, identifying and addressing any delays or bottlenecks
• Organize meeting activities, including setting agendas and documenting minutes, while facilitating cross-functional interactions

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 with rapid milestone achievement
• Preferred experience in standard project management processes and clinical trial management
• Knowledge of diagnostic and pharmaceutical industry practices is a plus