Supply Director

Director, Clinical Supplies | Oncology Biotech 🧬

New Jersey (Hybrid) 📍

Own and shape end‑to‑end clinical supply for late‑stage oncology trials 🎯

About the Company

This is a clinical‑stage oncology biotech focused on developing innovative, non‑surgical cancer therapies. The company has a growing pipeline spanning early development through late‑stage clinical trials, with increasing operational complexity as programs advance.

The organization operates in a lean, highly collaborative environment, where experienced operators are trusted to take ownership, make decisions, and directly influence trial success.

Why This Role

With several new oncology clinical protocols planned, clinical supply is a critical path function. The business is strengthening this capability by hiring a Director‑level Clinical Supplies leader to take full accountability for supply strategy and execution.

The Opportunity

This is a hands‑on, Director role with end‑to‑end responsibility for clinical supply across Phase 2/3 oncology studies.

You will be the primary owner of clinical supply, ensuring complex materials reach clinical sites on time, compliant, and without disruption, even as trial pressure increases.

What You’ll Do

• Own clinical supply strategy and execution across multiple oncology studies
• Manage forecasting, packaging, labeling, distribution, and IRT/RTSM
• Oversee external vendors and partners, holding them accountable on quality and timelines
• Partner closely with Clinical Operations, CMC, QA, Regulatory, and manufacturing partners
• Proactively identify and mitigate supply risks (expiry, temperature excursions, enrollment variability)
• Apply strong GMP/GCP judgment in a fast‑moving oncology development environment
• Reduce reliance on external support and help shape scalable supply processes

What They’re Looking For

• Senior ownership of clinical supply within oncology or specialty disease programs
• Experience supporting late‑stage (Phase 2b/3) clinical trials
• Hands‑on expertise across IRT/RTSM, forecasting, labeling, and vendor management
• Exposure to complex clinical supplies beyond simple oral IMPs
• Strong QA/GMP backbone with confidence to challenge and escalate when needed
• Comfortable operating independently in a lean, evolving biotech environment

Why It’s Interesting

• High autonomy and genuine ownership — effectively leading the oncology clinical supply function
• Direct impact on patient access to innovative cancer therapies
• Late‑stage oncology programs with real execution pressure
• Close partnership with senior clinical leadership
• Opportunity to leave a lasting operational footprint as the organization scales

If this sounds like a role where you could make a real impact, or you’d like to explore it confidentially, feel free to reach out.