Medical Director

i-Pharm Consulting; Australia; On-site; AUD 250,000 - 350,000; Full time

Job summary

A leading biotechnology firm based in Australia is looking for a Medical Director to shape the future of cancer care. This role requires a Medical Doctor with deep oncology experience to lead clinical strategy and trial execution across various oncology studies. Responsibilities include leading protocol development, engaging with global investigators, and providing scientific insights to optimize study execution. The ideal candidate will thrive in a collaborative, fast-paced environment and possess strong expertise in clinical trials.

Qualifications

• Experience leading protocol development for pivotal and early-phase oncology programs.
• Ability to engage globally with investigators and KOLs.
• Strategic thinker suited for a high-growth biotech environment.
• Strong knowledge of GCP and trial conduct.

Responsibilities

• Act as Medical Monitor and Safety Physician across oncology studies.
• Lead the development of clinical study protocols.
• Optimize study design and execution through scientific insight.
• Collaborate with Clinical Operations, Regulatory and R&D.
• Provide scientific and strategic input to optimise study design and execution.

Skills

Deep oncology or haematology-oncology experience

Clinical trial design

FDA/IND submission experience

Strong GCP knowledge

Collaborative mindset

Stakeholder collaboration

Education

Medical Doctor

Board Certification in Oncology

Job description

Medical Director – Oncology | Shape the Future of Cancer Care

Sydney, Melbourne or Brisbane based | Global High-Growth Biotech

A high-growth biotechnology company is pushing the boundaries of oncology drug development, with multiple programs advancing across solid tumours, AML and lung cancer. This role is ideal for a Medical Director who wants to combine scientific depth, strategic influence and hands‑on clinical impact.

Why This Role Matters

The Medical Director will play a central role in clinical strategy and trial execution. You’ll lead protocol development, engage investigators globally and help guide oncology programs through key stages of development. This is a position where your expertise directly shapes patient outcomes.

What You’ll Be Doing

• Act as Medical Monitor and Safety Physician across cutting‑edge oncology studies
• Lead protocol development for pivotal and early‑phase programs
• Build strong partnerships with global investigators and KOLs
• Collaborate closely with Clinical Operations, Regulatory and R&D
• Provide scientific and strategic insight to optimise study design and execution

Who We’re Looking For

• Medical Doctor (preferred) with deep oncology or haematology‑oncology experience
• Strong background in clinical trial design and protocol development
• Experience with FDA/IND submissions and IND programs
• Strategic thinker with strong GCP knowledge
• Collaborative mindset suited to a dynamic, fast‑paced biotech environment

For additional information, please contact [e-mail].

Only candidates deemed suitable will be contacted. Wishing you every success in your job search.