Clinical Science Specialist

Job Summary

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

Key responsibilities

• Coordinate project timelines, develop project plans, and track progress while identifying delays or bottlenecks
• Oversee sample process flow and ensure accurate reporting of results, implementing best practices within the clinical sciences team
• Organize and manage meeting activities, including setting agendas and documenting minutes

Required qualifications

• Minimum of 2 years of project management or clinical trial coordination experience in a regulated CRO, diagnostic, or pharmaceutical industry
• 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