Senior Medical Director, Oncology Clinical Development

GSK; Melbourne; Presencial; AUD 300.000 - 480.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Health care benefits

Retirement benefits

Paid holidays

Vacation

Paid caregiver/parental and medical/s.

Descripción de la vacante

GSK in Stevenage, UK, or other sites, seeks a Senior Medical Director for Oncology Clinical Development focused on GU cancers. You will lead clinical trials, engage with external experts, and drive strategic medical plans to support regulatory filings and market approvals.

The role requires on-site presence (minimum two days/week) and collaboration with cross-functional teams worldwide. Strong leadership and pharmaceutical development experience are essential.

Formación

• Medical degree and completion of advanced specialty training in Medical Oncology, Radiation Oncology, GU or related field.
• Experience in GU prostate cancer and global pharmaceutical/biotech environments.
• Proven leadership in GU Oncology drug development across Phases 1–3.

Responsabilidades

• Lead phase 1–3 interventional clinical trials across assets.
• Represent disease area strategy and medical affairs.
• Oversee protocol development aligned with Clinical Development Plan.
• Interpret study results and ensure safety, efficacy, and data integrity.

Conocimientos

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

Educación

Medical degree with advanced specialty training in Oncology or related field

Descripción del empleo

GSK in Stevenage, UK, or other sites, seeks a Senior Medical Director for Oncology Clinical Development focused on GU cancers. You will lead clinical trials, engage with external experts, and drive strategic medical plans to support regulatory filings and market approvals.

The role requires on-site presence (minimum two days/week) and collaboration with cross-functional teams worldwide. Strong leadership and pharmaceutical development experience are essential.