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Clinical Medical and Regulatory Director - فرصتنا دوت كوم Clinical Medical and Regulatory Director - فرصتنا دوت كوم
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    Clinical Medical and Regulatory Director

    Medical
    Algiers
    Based in Algiers with responsibility for Algeria

    Novo Nordisk is looking for a CMR Director Clinical Medical amp Regulatory who will develop amp support CMR strategy to support business growths address medical ambitions towards better treatment and manage the CMR organization in Algeria. We are looking for a passionate leader who understands our key mission of Changing Diabetes® and Changing Possibilities in Haemophilia®.

    About the department

    Novo Nordisk Algeria based in Algiers is part of the business area Africa and is one of the top 15 global markets for Novo Nordisk and among the Top 3 markets for International Operations. Novo Nordisk in Algeria is a market leader within diabetes and has a diverse portfolio of insulins amp Oral preparations for the treatment of diabetes besides products for the treatment of hemophilia amp growth disorders.

    The CMR department comprising of 45 employees are responsible for all clinical medical amp regulatory aspects of the business unit in Algeria.

    The job

    As a CMR Director you will be part of the Algeria management team and your key responsibilities will be to lead amp manage all clinical medical and regulatory operations of the affiliate in full compliance with local procedures national regulationsrequirements and corporate requirements.

    You will support all business opportunities and strategic objectives taking into account the midterm business needs besides leading amp coaching a high performing team to ensure that each function C M and R reaches its targets.

    You will support strategic plans for prescribers implement medical projects that support the affiliate in general insure medical communication with healthcare professionals and translate global medical affairs into affiliate operational plans.

    You will drive clinical development programs in close collaboration with regional and HQ to ensure high quality time and cost effectiveness

    You will manage regulatory intelligence legislation and guidelines within the pharmaceuticalhealthcare industry and local regulatory plans besides ensuring compliance amp RA activities aligned with local business demands.

    Qualifications

    The ideal candidate would have a University degree or postdoctoral degree in medicine 10 years’ experience in pharmaceutical industry of which 45 years should be in management of functionteam within medical affairs or clinical operations Broad understanding of medical affairs and requirements for affiliate medical affairs Experience in translating clinical evidence into strategies for successful product development and launch preparation Experience in engaging with regulatory bodies and drug safety Experience in conducting phase 3 clinical trials Experience in Diabetes amp Hemostasis area will be an advantage You should be fluent in both written and spoken French English Arabic is an advantage

    The following competencies complement the ideal profile Setting direction amp strategy High performing Leading amp coaching people Focused on what matters Business amp industry understanding Communicating with impact Making things happen and stakeholder relationships.

    Contact

    If you are interested in applying for the position please contact mqamnovonordisk.Com or apply through Novo Nordisk Career site.

    Deadline
    July 31 2015 http://ift.tt/1exsah5
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