THE ASSOCIATE DIRECTOR, GLOBAL LABELLING STRATEGY

The Associate Director, Global Labeling Strategy for Early Asset has overall accountability for initial creation and relevant updates to labeling documents (Target Label Profile (TLP), Company Core Data Sheet (CCDS), United States Package Inserts (USPI) and EU Summary of Product Characteristics (SmPC) for products registered via the centralized, Mutual Recognition or Decentralized Procedure.

Responsibilities :

Drive the labeling strategy to early development activities to ensure consideration of labeling in claims development programs.

Ensures that the labeling strategy is aligned with the overall product regulatory, registration, commercial and development strategy.

Drives labeling strategy in partnership with the Global Regulatory Team Leader in line with the overall regulatory strategy by providing labeling expertise (labeling regulations, and competitor analyses) for Target Product Labeling, CCDS, USPI and SmPC (Centralized / Mutual Recognition / Decentralized Procedure) for high or medium complex projects in the Development and Lifecycle Management (LCM) projects.

Serves as primary contact for cross-functional Labeling Team Member (CFLT), eg Global Regulatory Team Lead (GRTL), Medical Surveillance Team Lead (MSTL), Functional SMEs, Documentation Leads and Medical Writer, Dossier Lead and Submission Manager, also serves as interface for Country Regulatory Managers to support timely and quality submissions globally.

Contributes from the labeling perspective / labeling environment to Clinical Study designs, protocols, Investigator Brochures and Briefing Books.

Coordinates labeling activities of multifunctional contributors, reviewers and approvers and manages the label review and approval process to maximize speed and quality.

Ensures effective planning of all cross-functional labeling activities.

Reviews country labels to ensure labeling compliance and adequacy to the regulatory strategy.

Train and provide guidance for other Global Labeling Leads as needed.

Participates in / Leads key initiatives (Process Improvements, Development of new tools, technologies) to support efficient global label development and worldwide submissions and approvals.

Identifies opportunities to influence regulatory policy and climate with respect to labeling content.

Requirements :

Masters of Life Sciences or equivalent, with thorough understanding of scientific principles and at least 5 years of Labeling Experience (CCDS / USPI / SmPC) or Bachelor of Life Sciences and at least 7 years of Labeling / Regulatory Experience.

Knowledge of Global Labeling Guidances, Drug Development and Commercialization of prescription medicines.

Understanding of the dynamics and purpose of the Company Core Data Sheets (CCDS) and the implications of the CCDS.

A understanding of pharmaceutical drug development.

Previous experience with Health Authorities bodies

Proven understanding of the dynamics and purpose of the Target Product Labeling and Company Core Data Sheets (CCDS) and their implications

Experience in developing of Target Product Labeling Good understanding of worldwide regulatory guidelines and their applications for guidance for labeling.

Proven ability to understand regulatory implications of product strategy related to labeling development, assessment and management

Demonstrated ability to develop strong and positive working relationships across diverse teams and within a global environment

Ability to influence and lead a diverse group of Subject Matter Experts from a variety of disciplines and facilitate discussions and decision making

Experience in managing high to medium complex projects

Excellent project management, verbal and written communication skills

Keen attention to detail and accuracy, coupled with the ability to think strategically

Ability to assimilate clinical and scientific information and present it in a concise manner, and translate them into labeling content

Ability to think creatively and good excellent problem-solving skills

Time management skills.