Director, Medical Information & Content Approval, Vaccines

GSK • Upper Providence, PA

101d

About The Position

The Director, Medical Information & Content Approval, Vaccines plays a critical role in managing a team that ensures the US and global promotional and non-promotional content meets the highest standards of quality, scientific accuracy, balance, and compliance that meets the scientific needs of customers to help inform clinical care and formulary access decisions. This includes ensuring the adherence to internal GSK standards and applicable external regulations, including an understanding of the ABPI code of practice. This role supports the Sr. MI &CA Director to develop and execute the Medical Information and Content Approval strategy, including innovative digital MI solutions. The Director serves as an influential partner to Medical Affairs, Commercial and other key business stakeholders.

Requirements

• PharmD, MD, PhD, or equivalent.
• 6+ years of experience in the pharmaceutical industry.
• 4+ years of experience in medical writing and/or promotional review and approval.
• 4+ years of experience in customer-focused, problem-solving, and conflict resolution roles.
• Experience in people leadership, management and development.
• Experience working in a highly dynamic, changing, and matrixed environment.

Nice To Haves

• Experience communicating and translating evidence and customer insights to/with matrix team partners.
• Experience of working at both global and local country level.
• Experience in Vaccines.
• Experience influencing internal and external stakeholders on priorities and needs.
• Strong understanding of international Codes of Practice (FDA, IFPMA, EFIPIA, IPHA, ABPI, etc.).
• Experience in reviewing and approving promotional and non-promotional content.
• Ability to develop and maintain strong trusted relationships with internal stakeholders.
• Demonstrated customer-focus, problem-solving abilities, and strong conflict resolution skills.
• Strong clinical literature evaluation skills.
• Strong communication skills.

Responsibilities

• Lead and oversee the Global Medical Information and Content Approval Team for the Vaccines therapeutic area (TA).
• Contribute to the development and execution of the Global Medical Information and Content Approval strategic priorities, including digital solutions.
• Lead and manage team members to ensure performance objectives are met, providing mentorship and coaching.
• Mentor and develop team members, ensuring they have adequate training and tools.
• Act as a delegate of the Senior Director, Medical Information and Content Approval at Leadership team meetings.
• Accountable for MI launch readiness plans including planning and maintaining a robust MI database.
• Maintain a robust understanding of the ABPI Code of Practice and other regulatory guidelines.
• Ensure thorough and timely review of promotional and non-promotional US and global materials.
• Accountable for ensuring MI requirements of the payer strategy for the U.S are met.
• Partner with GMI Contact Centre Director/s to ensure MI CC staff are well trained on new products.
• Strategically partner with key global TA and US medical stakeholders.
• Ensure effective scientific exchange with external customers at important US and Global Congresses.
• Represent Medical Information and Content Approval on cross functional or medical leadership meetings.

What This Job Offers

• Job Type: Full-time
• Career Level: Senior
• Education Level: Ph.D. or professional degree
• Number of Employees: 5,001-10,000 employees