Manager, Site Start Up

About This Role

This role involves defining, developing, and delivering global site start-up plans for clinical trials. The manager will oversee data analysis, drive accurate forecasts, and lead a team in optimizing site activation processes within the pharmaceutical industry.

Responsibilities

• Define, develop, and deliver the Global Site Start Up Plan
• Oversee the analysis of clinical trial data for accurate study start-up forecasts
• Drive rapid, accurate, and data-driven study start-up forecasts, benchmarking, and planning
• Develop creative processes, methodologies, data, and technologies for Site Start Up Services
• Partner with Clinical Operations teams to improve overall site start-up metrics
• Provide guidance, oversight, and training to the Site Start Up team
• Ensure standards are applied to the study start-up process across project portfolios
• Guide the collection and analysis of all data to influence site start-up timelines
• Lead the site start-up team to implement the Site Start Up Plan
• Resolve escalated issues identified by the site start-up team in partnership with the Study Manager

Requirements

• BS degree or international equivalent in a life science
• 4+ years of experience in Clinical Operations, Project Management, study start up, and trial optimization within a pharmaceutical company, CRO or relevant industry vendor
• 2+ years of direct responsibility in site activation and managing the study start up processes of clinical research studies at a sponsor or CRO
• Proficiency with software models and database structures
• Expertise in principles driving country/site start up and study start up strategies

Qualifications

• BS degree or international equivalent in a life science
• 4+ years of experience in Clinical Operations, Project Management, study start up, and trial optimization, with 2+ years of direct responsibility in site activation and managing study start up processes.

Nice to Have

• Global SSU experience

Skills

* Required skills

Benefits