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    Director Medical Affairs - Paris, France - elemed

    elemed
    elemed Paris, France

    il y a 5 jours

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    Description

    Title: Director Medical Affairs

    Location: France (remote)

    Contact:

    The company

    Are you passionate about collaborative environments and innovative ways to integrate medical strategies? Do you dream of leading groundbreaking initiatives in the medical device industry?

    The Opportunity

    Are you ready to lead with purpose and give something back? As Medical Affairs Director, you'll lead all Medical affairs activities related to existing and

    future products, for Core markets in Western Europe region.

    This is a leadership role, and we are looking for leaders with a proven track record of developing and retaining high performing teams You'll be creating an environment of excellence, coaching and developing talent while ensuring strict adherence to compliance standards.

    You'll lead your team in crafting and implementing medical plans that align with corporate priorities. Your role involves fostering robust collaboration with scientific experts across various therapeutic areas. Your responsibilities extend to supervising medical activities throughout the pre-launch and post-launch phases, working closely with the Commercial team to drive success.

    Your responsibilities:

    • Initiate, supervise, and drive progress: Take the lead in directing and monitoring all medical activities, from clinical research to post-marketing studies and Investigators' Initiated Trials.
    • Shape strategic direction: Develop and execute plans that steer the course for new product initiatives, ensuring they align with our overarching goals.
    • Forge impactful partnerships: Cultivate relationships with Key Opinion Leaders (KOLs) and spearhead programs that add value to our medical endeavors.
    • Be the face of our company: Deliver compelling presentations to expert groups, societies, and regulatory bodies, both regionally and internationally.
    • Stay connected: Attend relevant conferences and scientific gatherings to expand our network within the industry and therapeutic areas.
    • Ensure alignment and compliance: Maintain coherence between our Core Markets and France medical strategies and global directives, adhering to internal SOPs, policies, and country regulations.
    • Support global communication: Collaborate with the Global Medical Communication and Information team to ensure seamless dissemination of crucial medical insights.
    • Manage resources effectively: Oversee the budget of our Core Markets and France medical division, optimizing financial allocations for maximum impact.
    • Nurture talent: Take a proactive approach to talent management, fostering growth and development within our team.
    • Cultivate excellence: Create an environment where medical and scientific brilliance flourishes, motivating and empowering employees while ensuring accountability.
    • Drive collaboration: Play a pivotal role within cross-functional teams, facilitating synergy and cooperation across departments.
    • Uphold a culture of compliance: Maintain and reinforce a culture where adherence to regulations and ethical standards is paramount.

    Your qualifications:

    • Leadership experience in a medical affairs role across a region/cluster/or business unit
    • Medical device experience
    • Track record building, developing and growing successful teams in medical affairs
    • French speaker

    If you are interested in this exciting role, please send your application directly to

    Please note: Due to the high volume of applications we sometimes receive, our team might not be able to contact each applicant individually regarding the status of their application. If you do not hear from us after 10 days, please consider your application unsuccessful.

    Key skills we recruit for:

    ISO 13485, 21 CFR 820, CE marking, MDR, Medical device regulation, MDD, medical devices, Digital health, 510 (K), PMA, Regulatory affairs, quality assurance, QA/RA, design quality, ISO 14971, combination devices, sterilisation, AIMDD , CER, PMCF

    __________________________________________________________________

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