Senior Global Clinical Trial Lead (Remote)

Parexel; Richmond (VA); Remote; USD 110,000 - 170,000; Full time

Job summary

Parexel in the United States is seeking a Senior Clinical Trial Manager to lead end-to-end global trials with a cross-functional team. You will own the operational plan, oversee budget, timelines, quality, and milestones, and manage CRO/vendor relationships and risk mitigation to deliver trials on time and within budget.

You will ensure regulatory compliance, participate in inspections and QA audits, and collaborate with diverse stakeholders. Travel up to 10% is expected as needed.

Qualifications

• BS/BA degree required.
• 7+ years of clinical research experience leading Phase 1-4 trials.
• 3-5 years direct experience leading end-to-end global trials.
• Experience overseeing CRO/vendor relationships and budgets.
• Excellent decision-making, analytical and financial management skills.
• Leadership in multifunctional matrixed and global environments.
• Proficiency with MS Office Suite and MS Project.

Responsibilities

• Lead the cross-functional trial team to deliver the operational plan.
• Accountable for end-to-end trial delivery, budget, timelines, quality and milestones.
• Oversee CRO/vendor identification, SOW creation, budget oversight and KPIs.
• Proactively ensure milestones are met and risks are mitigated.
• Ensure regulatory compliance and readiness for inspections and audits.
• Collaborate with multiple internal stakeholders and travel as needed (~10%).

Skills

Leadership

Budgeting

Project management

Communication

Problem-solving

Financial management

Team mentoring

Strategic thinking

Education

BS/BA degree

Tools

MS Office

MS Project

Budget tracking tools

Job description

Parexel in the United States is seeking a Senior Clinical Trial Manager to lead end-to-end global trials with a cross-functional team. You will own the operational plan, oversee budget, timelines, quality, and milestones, and manage CRO/vendor relationships and risk mitigation to deliver trials on time and within budget.

You will ensure regulatory compliance, participate in inspections and QA audits, and collaborate with diverse stakeholders. Travel up to 10% is expected as needed.