Motivated and hardworking Strategist accustomed to working in dynamic complex cross-functional teams and projects; Ambitious with 16 years of experience in Regulatory Affairs, Pharmaceutical Industry, Project Management, Regulatory Information Management System and Supply Chain Management. Aspires to work in an innovative dynamic work environment and to apply my experience in Project Management, Licensing, Logistics and Supply Chain Management and Regulatory Affairs fields.My extensive knowledge of Global Regulatory Affairs Submission Requirements, Strategies from Product Development Phase, CMC dossier, Labeling, Submission to health authorities and Response to inquiries to Post Approval Changes for New MA and Renewal files for Oncology, Biosimilars, Generic and NCE Applications gives me the ability to map new submission pathways and strategies to open new opportunities in new markets and successfully manage clients accounts to achieve submissions and approvals with minimum deficiencies and with fast track timelines. I have a strong Leadership, Team Management, Negotiation skills and significant experience in interacting with regulatory authorities in MENA with a proven record of mapping execution action plans for complex projects and successfully building and leading high performing teams through establishing new processes, SOP and KPIs for projects and functions.