Global Clinical Trial Manager: Strategy & Delivery

Parexel; Richmond (VA); On-site; USD 110,000 - 140,000; Full time

Job summary

Parexel is seeking a Clinical Trial Manager to oversee study-level activities, vendor oversight, and country/regional CRO delivery. You will align feasibility, set targets, conduct risk reviews, and address country challenges impacting study delivery.

Responsibilities include leading project teams, budgets, timelines, and training material development, with ~10% travel. Bachelor’s degree required and 5+ years CRO/pharma experience preferred.

Qualifications

• Minimum 5+ years of clinical research experience gained with a CRO, biotech or pharmaceutical company working on phase I-IV global clinical trials.
• 2-3 years leading aspects of global clinical trials.
• Experience working with CROs.

Responsibilities

• Manage integration of project team activities.
• Oversee study operations: regulatory submissions, drug supply, enrollment, timelines, budgets, data flow.
• Provide input on trial-level operational strategies from protocol to CSR.
• Contribute to global recruitment plans.
• Manage CRO/vendor identification, SOW creation, and budget oversight.
• Create and update critical trial documents.
• Support development of training materials.
• Review budgets, timelines, forecasts for studies.
• Support inspection readiness and risk mitigation.
• Participate in process improvements.
• Manage relationships with sites and vendors.
• Interface with internal stakeholders.
• Support onboarding of new team members.
• Attend stakeholder meetings and provide updates.

Skills

Decision making

Leadership

Cross-functional

Mentoring

Organization

Problem solving

Project management

Communication

Travel

Education

Bachelor's degree

Tools

MS Office Suite

Job description

Parexel is seeking a Clinical Trial Manager to oversee study-level activities, vendor oversight, and country/regional CRO delivery. You will align feasibility, set targets, conduct risk reviews, and address country challenges impacting study delivery.

Responsibilities include leading project teams, budgets, timelines, and training material development, with ~10% travel. Bachelor’s degree required and 5+ years CRO/pharma experience preferred.