Project Specialist (clinical experience)
Core
Managing clinical study timelines, budgets, and operational compliance for drug development trials.
Role type
Clinical Project Specialist
Builds
Clinical trial execution plans and operational workflows
Domain
Life sciences / Clinical research
Required skills
Clinical trial process knowledge, SOP/GCP compliance, site/vendor selection, budget management, cross-functional collaboration, recruitment strategy
Preferred skills
Clinical project management certification, GCP certification, Associate's degree in related field
Technologies
Microsoft Office Suite (Excel, Word, PowerPoint)
Responsibilities
Planning and directing clinical study timelines to meet milestones; Gathering input from cross-functional teams to create comprehensive plans; Ensuring consistency of clinical study processes by standardizing procedures; Overseeing operational aspects of clinical trials and ensuring compliance with SOP/GCP; Selecting sites and vendors and managing relationships; Preparing and monitoring clinical trial budgets; Monitoring progress and tracking KPIs; Implementing clinical development strategies; Developing trial recruitment strategies.
Seniority
Mid-level, hands-on IC