Medical Advisor - Respiratory

Medical Advisor - Respiratory

Sanofi

Stockholm, Sweden

Key Responsibilities

KTL and healthcare professional management:

  • Identify, develop and maintain collaborative relationships with current and future Swedish thought leaders within the Respiratory area (both upper and/or lower airway diseases);
  • Chair and drive Swedish expert meetings/advisory boards;
  • Establish KTL engagement plans and drive activities, including engagement with Swedish payers;
  • Be responsible for scientific/medical content in educational activities for Swedish KTL’s and healthcare professionals, e.g. through presentations at 1:1 meetings, investigator meetings, advisory boards and other relevant scientific meetings.

Clinical, medical and scientific support:

  • Identify, activate, support and maintain ISS’s;
  • Keep up to date with Sanofi's clinical activities and support and facilitate desired clinical trials;
  • Drive medical education of internal stakeholders and teams in Sweden;
  • Support Swedish field sales and efforts related to presenting clarity around clinical and scientific information;
  • Be a strong partner to the Immunology Business Unit, Medical Team (regulatory, PV, medical information) and Market Access in Sweden and provide continuous input, medical advice and training on request;
  • Based on ethical and legal standards in Sweden review and approve scientific and external communication materials, including marketing materials;
  • Support Market Access activities and provide medical and scientific input to applicable submissions.

General:

  • Provide updates on MEDAPP from relevant external scientific meetings, including international conferences;
  • Participate in continuous trainings regarding the Respiratory and Immunology area;
  • Ensure to be updated on the latest scientific information concerning Sanofi Respiratory products and to have a good knowledge about other current and emerging treatments for patients within this therapeutic area;
  • Keep current with relevant literature in the therapeutic area;
  • Participate in congresses, symposia and other relevant meetings;
  • Be actively responsible for self-development based on the organizational development needs, such as up to date knowledge of regulatory guidelines and standard operating procedures;
  • Adhere to regulations and compliance guidelines in all aspects of scientific dissemination of information;
  • Ensure that all promotion materials comply with company procedures, medical strategy, Swedish law and regulatory guidelines;
  • Actively take part of internal trainings and meetings.

About you

To excel in this role you will need to have:

  • Medical degree (preferred), or academic scientific, Pharm D, MSc and/or PhD in life sciences, or equivalent;
  • Knowledge of the pharma/biotech industry and relevant experience in a healthcare environment;
  • Clinical study and/or project management experience;
  • Proven Medical Affairs experience is an advantage;
  • Some experience in upper and/or lower airway diseases is a plus;
  • Self-motivated, organized and be able to work independently and as part of a team;
  • Ability to adapt to new procedures and software;
  • Capability for continuously update and follow scientific literature of relevance;
  • Excellent presentation skills and proficient in public speaking;
  • Possesses integrity and self-awareness;
  • Analytical whilst able to retain a broad perspective;
  • Ensures that projects, assignments and deadlines are completed on schedule;
  • Excellent command of both verbal and written English and Swedish;
  • Willingness to travel and attend external & internal meeting and trainings (5 -10 days per month or as required).

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© EuroJobsites 2020

EuroJobsites is a registered company number: 4694396 VAT number: GB 880 9055 04

Registered address: EuroJobsites Ltd, Unit 8, Kingsmill Business Park, Kingston Upon Thames, London, KT1 3GZ, United Kingdom

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