Medical Advisor (m/f/d) Speciality Care

Our client Swedish Orphan Biovitrum is an international speciality healthcare company dedicated to rare diseases. The product portfolio focuses primarily on haemophilia, inflammation, genetic and metabolic disorders. Furthermore the company is a pioneer in biotechnology with world-class capabilities in protein biochemistry and biologics manufacturing.


We are searching for Swedish Orphan Biovitrum as soon as possible for a dedicated and experienced

Medical Advisor (m/f/d) Speciality Care

  • Bereich:


  • Berufssparte:

    Medical Affairs

  • Arbeitsregion:

    Greater Munich area

  • Art der Anstellung:


  • Kennziffer:


  • Aktualisierung:


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Your tasks

  • Help bringing the newest Innovation of our client to the market in Germany, Austria and Switzerland from a medical affairs point of view
  • Be responsible for the conduct and project management of further studies to the assigned drug to ensure further line extensions
  • Organize and set up scientific advisory boards with the appropriate key stakeholders
  • Engage cross-functional in the AMNOG process incl. medical input in the value dossier, GBA Meetings and negotiation with the German GKV/PKV system
  • Be the first contact for the first line top ten KOLs and develop/maintain collaborative relationships with these in close collaboration with the marketing team
  • Deliver high quality medical and scientific communications as well stakeholder engagement plans in line with defined communication plans
  • Support country “Global Brand” team in developing local medical tactics and provide input to HQ/regional plans if relevant
  • Coordinate medical information enquiries in collaboration with the local organization and HQ
  • Attend relevant local, regional and global congresses and symposia to represent the company and interact with appropriate stakeholders and customers
  • Initiate, coordinate and support symposia at national congresses
  • Maintain and develop strong relationships with scientific societies and central decision makers at relevant local health authorities
  • Provide advice to the organization and management on medical matters and their legal implications
  • Safeguard that the medical and scientific knowledge for the therapeutic area remains at the forefront of contemporary thinking; remain updated on therapeutic trends related to new and existing products

Your qualifications

  • University degree in a medical or natural scientific discipline with a PhD
  • Professional experience of at least 3 years within the pharmaceutical industry as a member of medical affairs, clinical development, clinical research
  • Hands on experience within immunological, oncological therapies or orphan drugs
  • Experience from an international Life Science organization
  • Experience in organize medical advisory boards and symposia at national and international congresses
  • Experience in writing scientific publications.
  • Experience in developing scientific presentations and giving scientific lectures
  • Experience in initiation, coordinating and running study projects (ISS, PMS, Phase III trials)
  • Strong networker and teamplayer with proven ability to make own decision and take the responsibility
  • Already been part of an AMNOG process with responsibility to develop a value dossier and been the medical responsible person for the whole process (GB-A hearing and GKV-SV price negotiation)
  • Experience in communicating and building relations with authorities
  • In addition to German, fluency in English
  • Proficient user of modern IT and office software
  • Pro-active & action oriented; innovative and structured working style
  • Team player with self-dependent working style. Able to operate with minimal supervision

Ihr Ansprechpartner

Tilman Grumbd


Optares Medical GmbH & Co. KG
Tilman Grumbd
Heiligengeist Höfe 8
26121 Oldenburg