Lung Oncology Clinical Development Lead — Senior MD

GSK; Stevenage; On-site; GBP 180,000 - 240,000; Full time

Job summary

GSK is seeking a Senior Medical Director, Oncology Clinical Development – Lung, to provide medical oversight across studies and ensure safety and scientific integrity. The role requires strategic collaboration with CDL, cross‑functional teams, and external experts, with on‑site presence at Stevenage or Cambridge as timelines permit.

The position leads medical input on protocol development, safety monitoring, data interpretation, and programme‑level decisions within an oncology-focused clinical

Qualifications

• Medical degree with advanced oncology/haematology training.
• Experience leading lung cancer drug development programs.
• Clinical development expertise across multiple studies or programmes.
• Understanding of GCP, ICH and regulatory frameworks.
• Strong cross-functional leadership in matrix teams.

Responsibilities

• Serve as senior physician leader providing medical oversight across study design, conduct and data interpretation.
• Guide medical monitoring and safety oversight ensuring patient safety and clinical integrity.
• Interpret complex data to inform programme-level decisions and scientific positioning.
• Collaborate with cross‑functional teams to integrate medical considerations in study execution.
• Mentor Medical Directors and contribute to external scientific engagement.

Skills

Lung cancer drug development

Oncology clinical development

Clinical safety oversight

Cross-functional collaboration

Regulatory interactions

Education

Medical degree and advanced oncology/haematology training

Tools

GCP/ICH knowledge

Data interpretation

Job description

GSK is seeking a Senior Medical Director, Oncology Clinical Development – Lung, to provide medical oversight across studies and ensure safety and scientific integrity. The role requires strategic collaboration with CDL, cross‑functional teams, and external experts, with on‑site presence at Stevenage or Cambridge as timelines permit.

The position leads medical input on protocol development, safety monitoring, data interpretation, and programme‑level decisions within an oncology-focused clinical