Executive Director - Strategic Labelling

Executive Director - Strategic Labelling

Location
Upper Providence, Pennsylvania, USA – 200 Cambridge Park Drive, GSK HQ, Wavre

At GSK, we aim to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting‑edge technology to transform lives. We foster a culture of ambition for patients, accountability for impact, and the commitment to doing the right thing.

We are seeking an experienced and dynamic Executive Director, Strategic Labelling to lead global labelling development and governance for GSK’s diverse portfolio of medicines and vaccines. The role drives the initiation and development of labelling aligned with Target Medicine Profiles (TMP) and Target Vaccine Profiles (TVP) from early lifecycle stages through to commercialization. You will ensure labelling progresses seamlessly through project milestones and governance processes, while maintaining compliance with external regulations and GSK standards.

This role offers an opportunity to engage with senior stakeholders across R&D, Regulatory, Safety, and Commercial functions, fostering collaboration and innovation in labelling standards.

• Lead the global labelling process for GSK’s development portfolio through early lifecycle stages.
• Ensure regulatory requirements related to product information and submission strategies are met, proactively resolving issues across therapy areas.
• Provide strategic direction for labelling governance and represent GSK in global labelling committees and industry events.
• Advise senior management and regulatory teams on product labelling policies, standards, and compliance.
• Manage and motivate the Strategic Labelling team (including team leaders and their teams), fostering collaboration and alignment with GSK’s principles.
• Represent GSK in industry groups and during internal and external regulatory inspections or audits related to labelling governance and processes.

• Bachelor’s degree in Science, Medicine, or Pharmacy.
• Regulatory experience across all phases of the drug development process in a global pharmaceutical company.
• Global labelling experience.
• People management and matrix leadership experience.

• Advanced degree (MS, Pharm
  
  D, PhD) in Science, Medicine, or Pharmacy.
• Regulatory Affairs strategy experience, preferably in a leadership role.
• Deep understanding of multi‑regional external regulatory environments.
• Proven ability to rapidly assimilate data and resolve complex problems, making recommendations to senior management.
• Proven ability to lead global teams, resolve complex regulatory and scientific issues, and influence effectively in a matrix environment.
• Strong interpersonal, presentation, and communication skills with established internal and external networks.

If you are ready to lead labelling strategy that helps bring safe and effective medicines to patients worldwide, we want to hear from you. Apply now and tell us how your experience and values align with this role.

For candidates based in Cambridge, MA;
Waltham, MA;
Rockville, MD; or San Francisco, CA, the annual base salary ranges from $221,925 to $369,875. The US salary ranges reflect work location within the US market, the candidate’s skills, experience, education level, and market rate for the role. In addition, this position offers an annual bonus and eligibility to participate in a share‑based long‑term incentive program. Benefits include health care and other insurance benefits, retirement benefits, paid holidays, vacation, and paid caregiver/parental and medical leave.

Salary ranges are not displayed for all countries; relevant compensation will be discussed during the recruitment process. For more information about compensation and benefits, please visit GSK US Benefits Summary.

If you require adjustments to our application process to demonstrate your strengths and capabilities, contact HR.Americas

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