Managing Editor, Medical Devices
Clarivate
Barcelona, Spain
hace 6 días

Clarivate Analytics is a global leader in providing trusted insights and analytics to accelerate the pace of innovation.

We deliver critical data, information, workflow solutions, and deep domain expertise to innovators worldwide.

  • Our solutions cover the entire lifecycle of innovation : scientific and academic research; patent analytics and regulatory standards;
  • pharmaceutical and biotech intelligence; trademark, domain and brand protection. Our portfolio consists of some of the world’s most trusted brands, including Web of Science, Derwent, CompuMark, Cortellis, MarkMonitor, and Techstreet.

    We employ more than 4,300 colleagues in 43 countries.

    Clarivate Analytics is a public company. We are listed on the New York Stock Exchange under the tickers NYSE : CCC; CCC.WS.

    At Clarivate, we believe human ingenuity can transform the world and improve our future. That’s why we harness our global reach, curate our content, and invest in best-in-class technology and people.

    Join the team that is improving the way the world creates, protects, and advances innovation.

    Clarivate Analytics is the world’s leading source of intelligent information for businesses and professionals. We combine industry expertise with innovative technology to deliver critical information to leading decision makers in the financial, legal, tax and accounting, scientific, healthcare and media markets, powered by the world’s most trusted news organization.

    Our scientific knowledge and information is essential for drug companies to discover new drugs and get them to market faster, for researchers to find relevant papers and know what's newly published in their subject, and for businesses to optimize their intellectual property and find competitive intelligence.

    Today we are the established and authoritative pharmaceutical and biotechnology information resource, and the industry authority on the global generics market.

    Both innovators and generic manufacturers trust us because our integrated solutions contain an unrivalled breadth and depth of timely, relevant strategic information from multiple databases, delivered on powerful platforms, accompanied by intuitive analytical tools, and backed up by dedicated support teams.

    But we provide far more than just content sets. Our data are enriched with unique abstracts, commentaries and analysis prepared by our team of industry experts critical insight on-tap from the thought leaders that shape pharmaceutical opinion.

    All over the world, decision-makers depend on us for the essential knowledge that can justify their strategies, promote outstanding research and business growth, and keep them abreast of the market.

    You will work within the Life Science regulatory editorial team with primary responsibility for :

    1 / Regulatory surveillance for a given set of countries with focus on Medical devices

  • Maintaining up to the date the medical devices / IVD information in CRI
  • Analyzing the impact of drug / devices changing regulations to create and / or enrich CRI proprietary documents.
  • Supporting the Digital Health initiative by providing insight into the regulatory framework
  • Driving the content development for the Cortellis Regulatory Intelligence (CRI) country modules by interacting with local consultants and regulatory Agencies.
  • Monitoring agency and professional websites, local specialized press, conferences selecting documents to be integrated in line with CRI Scope and editorial processes
  • Contributing to Thought Leadership activities for the region.
  • 2 / Provide support to the team in place for the development of new content for Cortellis RI worldwide

  • Collaborate to regulatory projects / initiative for other than medical devices
  • Provide support to other teams (product team, editorial team, etc) if needed for questions, clarifications.
  • Perform quality check of the information published by the team and ensure harmonization of content
  • 3 / Customers / Sales support

  • Provide customer support for questions related to Medical Device field
  • Communicate new regulatory content to sales or product specialists.
  • Participate in webinars, client events if needed
  • Required skills / Experience :

  • Scientific degree, Engineer
  • Master or Regulatory experience in Medical Devices (>
  • 3 years)

  • Fluent in English
  • Project management skills.
  • Good problem solver and able to demonstrate good judgment in decision making and setting priorities.
  • Capability to work remotely with peers in an international environment
  • Team spirit and good communication skills.
  • 2 / Administrative tasks

    Management of contract with local consultants and Health Agency, investigation and negotiate copyrights, responsibility, follow-up and control of budget per module

    What We Can Offer To You

  • A start up culture / working environment combined with all the financial and stability advantages of working for a large PE backed business
  • An opportunity to have a real impact on the global Life Sciences industry
  • 30 working days of vacation
  • Active volunteering community, with 16 paid hours of volunteering time
  • Private Health and Life & Disability insurances.
  • Gym Sports Club Reimbursement
  • Tax-free benefits (Ticket Restaurant scheme, kindergarten and transport cards)
  • Agile work environment with a team of talented colleagues
  • On-site language classes (Catalan, Spanish and English)
  • Central office location in Barcelona (Next to Sagrada Familia) with global and dynamic employee base (more than 20 nationalities)
  • Free fresh fruit, coffee and tea
  • It is the policy of Clarivate to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, pregnancy, sex, sexual orientation, gender identity and / or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law.

    In addition, Clarivate will provide reasonable accommodations for qualified individuals with disabilities.

    Inscribirse
    Mi Correo Electrónico
    Al hacer clic en la opción "Continuar", doy mi consentimiento para que neuvoo procese mis datos de conformidad con lo establecido en su Política de privacidad . Puedo darme de baja o retirar mi autorización en cualquier momento.
    Continuar
    Formulario de postulación