Global Oncology Clinical Ops Lead (Remote)

Barrington James; United States; Remote; USD 180,000 - 230,000; Full time

Job summary

Barrington James is seeking an Associate Director, Clinical Operations (Oncology) to lead end-to-end global Phase 2/3 oncology studies, from start-up to close-out, in a remote-capable role.

You will manage CROs, budgets, timelines, and risk, mentor trial managers, ensure ICH GCP and FDA compliance, and partner across Clinical Development, Regulatory, Data Management, Biostatistics and Drug Supply. This is a hands-on leadership role for a fast-scaling biopharma with strong oncology programs.

Qualifications

• 8+ years of clinical operations experience in biotech, pharma or CRO.
• Strong oncology experience; hematology a plus.
• Proven track record delivering global Phase 2/3 studies, ideally registrational.

Responsibilities

• Lead planning and execution of global Phase 2/3 oncology trials, ensuring delivery to timeline, budget and quality.
• Select, manage and oversee CROs and vendors, holding partners accountable to performance metrics.
• Build and manage study budgets, timelines and risk mitigation plans.
• Drive site selection, start-up and enrolment strategy across the US and global regions.
• Partner with Clinical Development, Regulatory, Data Management, Biostatistics and Drug Supply.
• Ensure inspection readiness and compliance with ICH GCP and FDA requirements.
• Line manage and mentor Clinical Trial Managers and study team members.

Skills

Oncology operations

Clinical trial leadership

Vendor/CRO management

Budget management

Cross-functional collaboration

Regulatory compliance

Education

Bachelor’s degree in life sciences

Advanced degree preferred

Job description

Barrington James is seeking an Associate Director, Clinical Operations (Oncology) to lead end-to-end global Phase 2/3 oncology studies, from start-up to close-out, in a remote-capable role.

You will manage CROs, budgets, timelines, and risk, mentor trial managers, ensure ICH GCP and FDA compliance, and partner across Clinical Development, Regulatory, Data Management, Biostatistics and Drug Supply. This is a hands-on leadership role for a fast-scaling biopharma with strong oncology programs.