Remote Global Oncology Project Director

Pfm; Spain (TX); Remote; EUR 120,000 - 150,000; Full time

Job summary

Precision for Medicine is seeking an experienced Project Director for global, late-phase clinical trials in oncology. This fully remote role supports clients worldwide and leads cross-functional teams to plan, execute, and optimize studies from initiation through close-out.

You will manage budgets, timelines, risk mitigation, quality standards, and bids. The ideal candidate has 8+ years in clinical research, strong communication skills, and expertise with ICH-GCP and trial management systems.

Qualifications

• 8+ years of clinical research experience or equivalent.
• Direct project management experience (5+ years).
• Strong knowledge of ICH-GCP and industry SOPs.
• Experience managing global studies or portfolios.

Responsibilities

• Serve as primary client liaison for trials and proposals.
• Oversee all aspects of a clinical trial portfolio across studies.
• Provide direction to project managers on establishment, planning, initiation, procurement, execution and closeout.
• Manage study budgets and forecast to support business objectives.
• Develop robust project plans with risk management and contingency measures.
• Ensure Quality management and eTMF readiness across projects.
• Prepare status updates for clients and senior management.

Skills

Project management

Budget management

Cross-functional leadership

Client liaison

Risk management

Excellent communication

Education

Bachelor’s degree in science/health

Advanced degree preferred

Tools

Microsoft Office

Microsoft Project

eTMF

EDC

CTMS

Job description

Precision for Medicine is seeking an experienced Project Director for global, late-phase clinical trials in oncology. This fully remote role supports clients worldwide and leads cross-functional teams to plan, execute, and optimize studies from initiation through close-out.

You will manage budgets, timelines, risk mitigation, quality standards, and bids. The ideal candidate has 8+ years in clinical research, strong communication skills, and expertise with ICH-GCP and trial management systems.