Director, Regulatory Advertising and Promotion Policy- Oncology Job at GlaxoSmit

Site Name: USA - Pennsylvania - Philadelphia, USA - Massachusetts - Waltham, USA - North Carolina - Durham

Posted Date: Nov 27 2024

Are you passionate about regulatory advertising and promotion review with oncology experience? Within the Oncology space, we are in a period of very dynamic growth, as we continue to expand and develop our pipeline and portfolio. We are looking for a driven and motivated regulatory professional who will be instrumental in supporting the growth of our expanding oncology portfolio.

As the Director, Regulatory Advertising & Promotion Policy, you will be responsible for leading assigned products providing sound regulatory advice for advertising and promotion of prescription drug products and biologics that minimizes the risk of regulatory action, competitively positions assigned products and is consistent with applicable FDA regulations and GSK policy.

This role will act as a credible, influential, respected spokesperson for assigned products during interactions with the Office of Prescription Drug Promotion (OPDP) and/or the Advertising and Promotional Labeling Branch (APLB) reviewers. The Director will provide consultative support to Global Regulatory Affairs therapeutic project teams for issues/strategies relating to continuity between development plans and commercial objectives.

Key Responsibilities:

This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following:

1. Provide strategic and operational leadership to Marketing Brand Teams, Legal, Medical Affairs and Clinical in the development of advertising and promotion for the US market (for major company assets) in accordance with business goals and objectives, FDA regulation, PhRMA guidelines and company policy
2. As an internal expert on FDA regulations governing promotion, maintain awareness of evolving regulations and interpretations, advisory comments, enforcement letters and policy issues, and communicate relevant information appropriately to stakeholders
3. Establish and nurture a productive, transparent relationship with OPDP and/or APLB to achieve successful and timely review of advisory submissions and effective resolution of regulatory actions.
4. Advise on the development of US labeling to ensure support for anticipated promotional messages and claims
5. In-depth understanding of labeling for assigned GSK and competitor products and the subsequent translation of that knowledge into the development of promotional materials
6. Competitively position promotional materials that comply with applicable FDA and corporate regulations, policies and guidance
7. Influential member of multiple cross-functional US Pharma, Regulatory Matrix Teams and R&D teams with senior membership
8. Identify continuous improvement opportunities
9. Participate in company working groups that focus on advertising and promotion standards and guidelines
10. Serve as regulatory advertising and promotion lead on cross-functional matrix teams supporting early pipeline assets and pre-launch products for future promotional impact. Provide strategic advice on early assets, launch, and lifecycle product activities (e.g., clinical trial protocols, substantiation for claims, labeling review).

Why you?

Basic Qualifications:

We are looking for professionals with these required skills to achieve our goals:

• 5 or more years of regulatory experience in the development of Pharmaceutical advertising and promotion for the US market (for major company assets)
• Prior work experience interacting with OPDP and/or APLB reviewers
• Experience working on pre-launch activities and launch promotional campaigns
• Experience facilitating groups of individuals to work together on creating solutions

Preferred Qualifications:

• Advanced degree in biological or health care scientific discipline
• 7 or more years of regulatory experience working on multiple products across a range of therapeutic areas.
• Experience supporting Oncology products and experience in advanced areas of science, e.g., Immuno-oncology.
• Demonstrated history of successful interactions with OPDP and/or APLB reviewers
• Experience providing regulatory ad/promo consultations on target medicine profile, clinical trial designs and during labeling development
• Consistent ability to foster strong matrix working.
• Proven track record of facilitating groups of individuals to work together on creating solutions
• Ability to manage and execute on projects independently, with minimal supervision
• Awareness/familiarity working with the digitalization in development and regulatory strategy to enhance decision-making, and drive efficiency and innovation
• Excellent communication skills, both written and verbal

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