Global Head of Labelling Strategy & Oncology Governance

1925 GlaxoSmithKline LLC; Upper Providence (Delaware County); Hybrid; USD 222,000 - 370,000; Full time

Benefits offered by this job

Health insurance

Retirement benefits

Paid holidays

Vacation

Parental and medical leave

Job summary

GSK is seeking a therapeutic head within Labelling Strategy and Governance to lead a global oncology labelling team. You will shape clear, compliant labelling and align with R&D stakeholders to support patient care and product success.

Ideal candidates have senior regulatory experience, cross-functional leadership, and a track record in developing patient-focused labeling. This hybrid role offers visible impact and opportunities to advance global labelling standards.

Qualifications

• Bachelor’s degree in life sciences, pharmacy, medicine, or related field.
• At least 5 years of regulatory affairs or labelling experience in pharma/biotech with line and matrix leadership.
• 3+ years leading global labelling development, submissions, or regulatory interactions.

Responsibilities

• Manage, train, and motivate a team of global labelling professionals for the oncology portfolio.
• Oversee labelling process for development portfolio from early development to early lifecycle.
• Ensure regulatory compliance and work with matrix teams to resolve issues proactively.
• Provide strategic direction for labelling governance and serve on Global Labelling Committee.
• Advise Regulatory and senior management on labelling issues with cross-functional interfacing.
• Engage with Regulatory Authorities to drive innovative labelling approaches.

Skills

Cross-functional leadership

Regulatory affairs

Labelling strategy

Stakeholder management

Regulatory compliance

Education

Bachelor’s degree in life sciences, pharmacy, medicine, or related field

Advanced degree (MS, PharmD, MD, or PhD) in a relevant discipline

Job description

GSK is seeking a therapeutic head within Labelling Strategy and Governance to lead a global oncology labelling team. You will shape clear, compliant labelling and align with R&D stakeholders to support patient care and product success.

Ideal candidates have senior regulatory experience, cross-functional leadership, and a track record in developing patient-focused labeling. This hybrid role offers visible impact and opportunities to advance global labelling standards.