דרושים ל.י.א.ל כח אדם

Manages the strategy, coordination, compilation and submission of new product applications, investigational new product applications and post approval supplements to the regulatory agencies.
Ensures compliance with global health authority regulations and interpretations. repares responses to regulatory agencies' questions and other correspondence.
Gathers and assembles information necessary for submissions in accordance with regulations and relevant guidelines. Involved with the preparation of necessary outlines, summaries, status reports, memos, graphs, charts, tables, and slides.
Provides solutions to a variety of problems of moderate scope and complexity. Organizes and maintains reporting schedules for new product application and investigational new product applications.
Leads and develops a team of regulatory affairs professionals in furtherance of the duties and responsibilities of