# Therapeutic Head, Labelling Strategy and Governance

**Company**: GSK
**Location**: Upper Providence, Pennsylvania
**Work arrangement**: hybrid
**Experience**: senior
**Job type**: full-time
**Salary**: $221,925 to $369,875
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://gsk.wd5.myworkdayjobs.com/en-US/GSKCareers/job/USA---Pennsylvania---Upper-Providence/Labelling-Strategy-and-Development--Oncology-Team-Lead_435545?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/job/therapeutic-head-labelling-strategy-and-governance-05344e3e-2ae/

## Description

As a therapeutic head within Labelling Strategy and Governance, you will lead a global labelling team for oncology products. You will engage with key stakeholders across R&D to ensure effective development of GSK oncology labels. You will shape labelling that is clear, compliant, and supports patient care and product success.

Responsibilities:

- Manage, train, and motivate a team of global labelling professionals for the oncology portfolio.

- Accountable for management of the GSK labelling process for the development portfolio from early development through to early lifecycle management.

- Ensure compliance with regulatory requirements and work with matrix teams to resolve issues in a proactive manner.

- Provide strategic direction for labelling governance issues for assigned therapeutic area and serve on Global Labelling Committee.

- Advise Regulatory and senior management on issues relating to product labelling.

- Engage with Regulatory Authorities in areas impacting labelling standards and policies.

Requirements:

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

- At least 5 years of regulatory affairs or labelling experience in the pharmaceutical or biotech industry with line and matrix leadership experience.

- 3+ years of experience leading global labelling development, submissions, or regulatory interactions.

Preferred Qualifications:

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

- Experience in oncology therapeutic areas and familiarity with oncology clinical data and endpoints.

- Prior direct experience interacting with regulatory reviewers.

- Experience aligning labelling strategy with commercial and medical affairs objectives.

- Track record of developing patient-focused labeling and plain-language content.

- Experience mentoring colleagues and building capability within a labelling or regulatory team.

Benefits:

- Health care and other insurance benefits.

- Retirement benefits.

- Paid holidays.

- Vacation.

- Paid caregiver/parental and medical leave.

Salary:

- $221,925 to $369,875 per year (for US locations)

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## Skills

### Required
- Pharmaceutical Regulatory Compliance
- Regulatory Strategies
- Resource Management
- Stakeholder Management
- Communication
- Matrix Leadership

### Nice to have
- Oncology
- Labelling Strategy
- Regulatory Affairs
- Leadership

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