Clinical, Medical & Regulatory Head, Morocco

Category: Clinical Development

Location:Casablanca, Casablanca-Settat, MA

• Implement and align medical affairs strategies with global and regional strategies and harmonize with medical projects and training across the affiliate to aids sales and marketing functions.
• Ensure the execution of clinical trials in the affiliate according to (Novo Nordisk) NN SOP’s, The International Council for Harmonization of Technical Requirements (ICH) Good Clinical Practice (GCP), and local regulations, and ensure timely submission and approval of product registrations.
• Represent the affiliate in regional and, where relevant, global boards/meetings and contribute the strategic KOL development plans for prescribers.
• Implement medical projects that aid overall business objectives and facilitate medical communication with healthcare professionals. Translate global medical affairs and regulatory strategies into regional operational targets.
• Ensure the implementation and maintenance of the Pharmacovigilance System for marketed products, clinical trial products, and technical complaints. Develop and manage the affiliate CMR strategy (short, medium, and long term) and performance. Ensure CMR competencies and alignment across the affiliate.

• A University degree in a relevant area, such as an MD, Pharma D, or Ph.D. degree in Life sciences.
• Min 10 years of professional experience in the research-based pharmaceutical industry in the field of medical-pharmaceutical information. Experience in the Diabetes & Haemostasias area are an advantage.
• Strong Leadership skills and sound medical-scientific understanding of medical affairs and requirements for regional medical affairs
• Significant experience in translating clinical evidence into strategies for successful product development and launch preparation

• English proficiency with functional area and proficiency in Arabic & French is a must have.