Global Clinical Trial Program Manager

Parexel; Helena (MT); On-site; USD 120,000 - 180,000; Full time

Job summary

PAREXEL is seeking a Clinical Trial Manager to oversee study-level operations across global CROs and vendors, ensuring alignment on feasibility, risk management, timelines, and regulatory deliverables. You will create and update trial documents, manage budgets, and drive country-level operational delivery.

The role requires 5+ years in clinical research, experience with CROs, and strong leadership in matrixed environments. Travel about 10% may be required; bachelor's degree is required.

Qualifications

• Minimum 5+ years of clinical research experience with a CRO/biotech or pharmaceutical company.
• 2-3 years leading aspects of global clinical trials.
• Experience working with CROs and global study delivery.

Responsibilities

• Manage integration of project team activities across studies.
• Oversee study sites, regulatory submissions, drug supply, enrollment and data flow.
• Provide input on trial-level operational strategies from protocol design to final report.
• Manage CRO/vendor identification, SOX creation, budgets, and day-to-day oversight.
• Create and update critical trial documents and training materials.
• Review budgets, timelines, and forecasts; support inspection readiness.

Skills

Leadership

Decision making

Problem solving

Communication

Cross-functional teamwork

Global environments

Education

Bachelor's degree

Tools

MS Office Suite

Job description

PAREXEL is seeking a Clinical Trial Manager to oversee study-level operations across global CROs and vendors, ensuring alignment on feasibility, risk management, timelines, and regulatory deliverables. You will create and update trial documents, manage budgets, and drive country-level operational delivery.

The role requires 5+ years in clinical research, experience with CROs, and strong leadership in matrixed environments. Travel about 10% may be required; bachelor's degree is required.