Clinical Trial Manager - Lead Strategy & CRO Oversight

Parexel; Montpelier (VT); On-site; USD 110,000 - 150,000; Full time

Job summary

Parexel in Montpelier, VT is seeking a Clinical Trial Manager responsible for study-level execution, including creating trial documents, vendor oversight, and CRO delivery across countries and regions.

You will manage integration of project team activities, study sites, regulatory submissions, drug supply, enrollment, timelines, budgets, and data flows, while providing input on operational strategies from protocol design to final study report.

Qualifications

• 5+ years in clinical research with CRO/biotech/pharma, global trials experience preferred.
• 2-3 years leading aspects of global clinical trials.
• Experience working with CROs.

Responsibilities

• Manage integration of project team activities
• Study sites and tracking systems for regulatory submissions, drug supply, enrollment, timelines, budgets and data flow
• Provide input on trial-level operational strategies from protocol design to final study report
• Provide input into global subject/patient recruitment plans
• Manage CRO/vendor identification and day-to-day oversight
• Create and update critical trial documents
• Support development of training materials
• Review budgets, timelines and forecasts
• Support inspection readiness activities including risk management
• Participate in process improvements at trial and department level
• Manage relationships between study sites and vendors
• Interface with internal stakeholders
• Support onboarding of new team members
• Attend stakeholder meetings and provide progress updates

Skills

Decision making

Leadership

Project planning

Communication

Travel

Stakeholder management

Education

Bachelor's degree

Tools

MS Office Suite

Excel

Word

PowerPoint

Job description

Parexel in Montpelier, VT is seeking a Clinical Trial Manager responsible for study-level execution, including creating trial documents, vendor oversight, and CRO delivery across countries and regions.

You will manage integration of project team activities, study sites, regulatory submissions, drug supply, enrollment, timelines, budgets, and data flows, while providing input on operational strategies from protocol design to final study report.