Medical Advisor Critical Care Germany

Neu-Isenburg, HE, DE, Germany

Job Description

Tätigkeitsbereich:

Regulatory & Medical

Veröffentlichungsdatum:

18.12.2025

Arbeitsort:

Neu-Isenburg 63263, Hessen, Deutschland, hybrides Arbeitsmodell

Vertragsart:

Dauerhaft, office based contract

Stelle ID:

4074



Beschreibung der Rolle

Medical Advisor - Critical Care - Germany





The role

The Medical Advisor, under the supervision of the Medical Lead, is responsible for development, execution and delivery of the Medical Affairs plan(s), and for provision of scientific input into brand strategy for GBU Critical Care in Germany.

The Medical Advisor will have a pivotal role in engaging with key internal and external stakeholders and for identifying national/local advocates through their engagements with Key External Experts (KEEs).



Your responsibilities

Medical Affairs Leadership




Maintain up-to-date scientific knowledge and understanding of the local market access and health care system to help to shape medical strategy and support broader business plans Proactively contribute medical & clinical expertise and insights to the development of the brand strategy for thrombosis therapeutic area Present the clinical data set for assigned product(s) at meetings e.g. Ad Boards, Investigator meetings, KEE meetings, CME & medical society meetings as appropriate (and according to local regulations) Work closely with KEEs to develop and drive the medical strategy and provide medical direction to the brand plan



Performance & Delivery




Lead development of local medical communication/publications, KEE, evidence generation plans for assigned product(s) aligned to Global plans and country brand plans. Organize and conduct medical education, scientific exchange and advisory board meetings (according to local regulations) Conduct local medical competitive intelligence and interpretation and share these with relevant internal stakeholders Develop/refine scientific content for medical tools & training, medical presentations, KEE decks etc. in alignment with those from GMA, global medical materials, country specific medical education strategy Create and deliver product training to the MSL team and other functions within the TA as appropriate (e.g. sales & marketing)



Governance & Compliance




Promotional review/compliance: Act as medical reviewer for activities and promotional materials in accordance with local compliance guidelines Ensure scientific and medical accuracy of outgoing materials, research papers and other reports, and may have sign off authority.



Collaboration & Partnership




Collaborate closely with internal LEO stakeholders – GMA, BU/marketing, market access, regulatory, medical information, patient safety and clinical operations, as needed Develop and enhance professional relationships with stakeholders including, professional societies and patient organizations; understand and address data gaps and unmet needs of these external stakeholders.




Your profile


Experience




Qualified to MD, PhD or PharmD level preferred Minimum of 5 years of experience within the pharmaceutical industry Minimum of 3 years Medical Affairs experience Experience in Critical Care TA preferred Good business/commercial understanding Excellent command of written and spoken English and local language(s) Track record of collaboration with commercial, legal, regulatory, and medical communications teams Profound knowledge of the local healthcare and market access system Experience and successful track record of liaising with HCPs Comprehensive knowledge of the legal and ethical framework and the procedural guidelines that apply to the promotion and approval of medic-inal products in the country.



Competencies




Goal orientated, with a history of meeting deadlines and objectives. Strong planning and organization orientation Ability to build and maintain relationships Exhibits a culture of integrity, excellence, initiative, and compliance Exceptional communication and presentation skills, including communi-cating complex scientific, or medical information to broad audience types High-level of scientific knowledge and ability to analyze and process complex clinical and scientific data and the ability to translate this into relevant and impactful local tactics and tools Quick self-learner, ability and willingness to work in a team and inde-pendently. Planning and prioritizing work to meet commitments aligned with organi-zational goals


Über die Haut hinaus





Schließen Sie sich LEO Pharma, einem weltweit führenden Unternehmen in der medizinischen Dermatologie, an, wenn wir über die Haut hinausgehen, um eine nachhaltige Wirkung zu erzielen. Unser innovativer Ansatz zeichnet uns aus. Wir setzen uns dafür ein, ein Vermächtnis zu hinterlassen, das sich positiv auf Patienten, Kollegen und unseren Planeten auswirkt.



Bei LEO Pharma glauben wir an die Kraft des Einzelnen, den Wandel voranzutreiben. Unsere flache Organisationsstruktur ermöglicht es Ihnen, sichtbare Wirkung zu erzielen und bietet vielseitige Rollen für die berufliche Weiterentwicklung. Wir schätzen Vielfalt und begrüßen Bewerbungen von allen qualifizierten Kandidaten, da wir wissen, dass unsere unterschiedlichen Perspektiven, Hintergründe und Einstellungen es uns ermöglichen, die besten Entscheidungen zu treffen. Werden Sie Teil unseres leidenschaftlichen Teams bei LEO Pharma und seien Sie Sie selbst, während wir zusammenarbeiten, um etwas zu bewirken.



Für bestimmte Positionen könnte LEO Pharma eine Hintergrundprüfung abschließen, die von einem Dritten durchgeführt wird.



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Job Detail

  • Job Id
    JD4085958
  • Industry
    Not mentioned
  • Total Positions
    1
  • Job Type:
    Full Time
  • Salary:
    Not mentioned
  • Employment Status
    Permanent
  • Job Location
    Neu-Isenburg, HE, DE, Germany
  • Education
    Not mentioned