Athsai ยท 3 hours ago
Global Labeling Strategist
United States
Full-time
Remote
Mid, Senior Level
5+ years exp
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Hiring Manager
Upma Ghai CertRP
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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 for high complex projects in the Development and Lifecycle Management (LCM) projects.
Serves as primary contact for cross-functional Labeling Team Member (CFLT), e.g. 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.
Qualification
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Required
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 Guidance, 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
Good knowledge 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
Company
Athsai
Welcome to Athsai, a trailblazing force at the intersection of technology and talent.
2-10 employees
Funding
Current Stage
Early StageCompany data provided by crunchbase
