Oncology Regulatory Lead — Global Strategy & Approvals

Gsk; Stevenage, Cambridge; Hybrid; GBP 90,000 - 160,000; Full time

Job summary

GSK is seeking a Regulatory Affairs Manager in Oncology to lead global regulatory strategies and ensure compliant submissions across regions. The role involves collaboration with global teams, local affiliates and RA leads to shape development plans and drive successful approvals.

The position can be based in London or Stevenage with a hybrid work pattern. A strong background in oncology regulatory affairs and global submissions is required.

Qualifications

• Bachelor's degree in biological, pharmaceutical or healthcare science.
• Proven experience in drug development process, preferably in regulatory affairs and oncology.
• Knowledge of clinical trial and licensing requirements in major regional/global markets.
• Strong written and verbal communication skills for clarity and impact.
• Experience working effectively in matrix teams.

Responsibilities

• Develop and execute global regulatory strategies for oncology assets.
• Collaborate with cross-functional teams to align regulatory plans with strategies.
• Support interactions and submissions with regional authorities for development and approvals.
• Assess regulatory intelligence to inform strategy and decision-making.
• Ensure compliance with regulatory requirements throughout product lifecycle.
• Drive process improvements and strategic changes.

Skills

Regulatory Affairs

Oncology

Global strategy

Regulatory submissions

Cross-functional teamwork

Education

Bachelor's degree in biological, pharmaceutical or healthcare science

Job description

GSK is seeking a Regulatory Affairs Manager in Oncology to lead global regulatory strategies and ensure compliant submissions across regions. The role involves collaboration with global teams, local affiliates and RA leads to shape development plans and drive successful approvals.

The position can be based in London or Stevenage with a hybrid work pattern. A strong background in oncology regulatory affairs and global submissions is required.