Overview
Join to apply for the Director, Medical Information & Content Approval, Vaccines role at GSK.
Site Location information includes USA (Pennsylvania Upper Providence), Belgium (Wavre), GSK HQ, USA (North Carolina Durham).
Key Responsibilities
* Lead and oversee the Global Medical Information and Content Approval Team for the Vaccines therapeutic area, serving as subject matter experts for their products within the broader medical organization.
* Contribute to the development and execution of global MI and Content Approval strategic priorities, including digital solutions, to meet internal/external stakeholder information needs.
* Lead and manage team members to meet performance objectives, provide mentorship and coaching, and support development.
* Mentor and develop team members, ensuring adequate training and tools, and facilitate professional development through differentiated development plans.
* Act as a delegate of the Senior Director at Leadership team meetings as required.
MI and Content Approval
* Accountable for MI launch readiness plans, including maintaining a robust MI database to inform clinical decision making by healthcare professionals.
* Maintain up-to-date understanding of ABPI Code of Practice and other regulatory guidelines; escalate as appropriate.
* Ensure thorough and timely review of promotional and non-promotional US and global materials for scientific accuracy, rigor, fairness, and compliance.
* Ensure MI requirements of the payer strategy for the U.S. are met.
* Partner with GMI Contact Centre directors to ensure staff are trained on new products or new data in a timely manner.
* Collaborate with Legal, Medical, Clinical, Regulatory, Commercial and other stakeholders to ensure high-quality, audience-relevant content.
* Support MI content creation, medical review and approval, and onboarding of new team members as needed.
Cross-functional Collaboration
* Strategically partner with global TA and US medical stakeholders to align MI with the medical strategy of high-priority assets and meet HCP needs worldwide.
* Drive scientific exchange with external customers and support MI activities at major US and Global congresses using digital solutions.
* Represent Medical Information and Content Approval in cross-functional or medical leadership forums within the TA area.
Qualifications
Basic Qualifications
* PharmD, MD, PhD, or equivalent.
* 6+ years of experience in the pharmaceutical industry.
* 4+ years in medical writing and/or promotional review and approval.
* 4+ years in customer-focused, problem-solving, and conflict resolution roles.
* Experience in people leadership, management and development.
* Experience in a dynamic, matrixed environment.
Preferred Qualifications
* Experience translating evidence and customer insights to matrix partners; ability to develop innovative, customer-focused medical solutions.
* Experience working at global and local country levels.
* Experience in Vaccines.
* Ability to influence stakeholders and address scientific data gaps.
* Strong understanding of international Codes of Practice (FDA, IFPMA, EFPIA, IPHA, ABPI, etc.).
* Experience reviewing and approving promotional and non-promotional content.
* Ability to build trusted relationships with internal stakeholders.
* Strong clinical literature evaluation and communication skills.
GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, pregnancy, gender identity, sexual orientation, parental status, national origin, age, disability, or genetic information. If you require accommodation to apply for a job at GSK, please contact the GSK Service Centre.
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