Senior Oncology Medical Director – Clinical Development

GSK; Melbourne; On-site; AUD 300,000 - 540,000; Full time

Benefits offered by this job

Health care and other insurance

Retirement benefits

Paid holidays

Vacation

Paid caregiver/parental and medicalle

Job summary

GSK is seeking a Senior Medical Director, Oncology Clinical Development to lead phase 1–3 oncology trials. You will shape disease area strategy, manage clinical programs, and drive high‑quality data for regulatory submission and lifecycle management.

You will collaborate with internal experts and external thought leaders to advance priority assets and patient outcomes. This on‑site role requires presence at listed sites and offers leadership opportunities, a collaborative culture, and a

Qualifications

• Medical degree and completion of advanced specialty training in Medical Oncology, Radiation Oncology, GU or Internal Medicine with GU/oncology experience.

Responsibilities

• Lead phase 1–3 interventional clinical trials in oncology and oversee program development.
• Represent Clinical Development on disease area strategy and regulatory affairs alignment.
• Oversee protocol development to determine efficacy, safety, and product differentiation.
• Interpret and summarize study results for safety and efficacy and align with regulatory plans.
• Collaborate with external experts, investigators, and cross-functional teams to drive development.
• Author clinical study reports and regulatory documents; support health authority queries.

Skills

Clinical Data Interpretation

Clinical Pharmacology

Clinical Trial Designs

Clinical Trials Monitoring

Digital Fluency

Drug Development

Drug Regulatory Affairs

Evidence Based Decision Making

Executive Presence

Hematology and Oncology

Learning Agility

Matrix Leadership

Real World Evidence

Scientific Presentations

Strategic Direction

Education

Medical degree with advanced specialty training in Medical Oncology, Radiation Oncology, GU or Internal Medicine

Job description

GSK is seeking a Senior Medical Director, Oncology Clinical Development to lead phase 1–3 oncology trials. You will shape disease area strategy, manage clinical programs, and drive high‑quality data for regulatory submission and lifecycle management.

You will collaborate with internal experts and external thought leaders to advance priority assets and patient outcomes. This on‑site role requires presence at listed sites and offers leadership opportunities, a collaborative culture, and a