Director (m/f/d) Global Medical Affairs

with a focus on Clinical Evidence

Our client is one of the most promising biotech companies in the market for oncology and immunology with an outstanding pipeline of over 100 indications with numerous new drug candidates.

 

To launch the first product and prepare the next products in line for this step we are looking for a dynamic and scientific focussed

Director (m/f/d) Global Medical Affairs

with a focus on Clinical Evidence

  • Bereich:

    Medical

  • Berufssparte:

    Medical Affairs

  • Arbeitsregion:

    Greater Munich Area

  • Art der Anstellung:

    Permanent

  • Kennziffer:

    26496

  • Aktualisierung:

    10.03.2021

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Your tasks

  • Lead / co-lead Evidence Generation and Medical Communication initiatives supporting the launch of a new product in the area of hematology/oncology.
  • Work closely with Clinical Development as well as Commercial teams to support the execution of the launch and life cycle management strategies, ensuring internal and external launch readiness.
  • Contribute to gaining medical insights through routine KOL engagement and advisory boards.
  • Support adaptation of training and other scientific material, in collaboration with Marketing and other appropriate internal stakeholders.
  • Develop scientific education and in-house training for MSLs and other appropriate staff, as required.
  • Contribute to publication planning, and coordinate congress reporting and summaries; collect data on competitors and market development.
  • Review and critically appraise scientific literature to provide support and advice to medical and marketing groups. Adhere to and advise on compliance requirements, including prudent interpretation of the Code of Practice.
  • Support the companies development of positioning as a scientific authority in Non-Hodgkin’s Lymphoma.
  • Support development of KOL advocacy, through the provision of scientific and clinical information.
  • Build strategic partnerships with KOLs to ensure that the companies portfolio is appropriately positioned in treatment guidelines and protocols, through the provision of balanced, scientific information.
  • Ensure HCP and educational activities are of a high scientific quality and standard.
  • Prepare tailored clinical data packages for advisory boards, investigators, and other KOLs’ requests, to deliver scientifically credible messages.
  • Provide guidance regarding appropriate speakers for national/international congresses and workshops, in order to expand and enhance legitimate scientific exchange.
  • Develop and implement publication plans.
  • Facilitate and support the conduct of investigator-sponsored work (IST/IIT).  Support the approval and implementation of these projects in line with relevant pharmaceutical regulations and internal SOPs, as appropriate.
  • Develop and execute phase IV and observational studies

Your qualifications

  • Minimum 3-7 years relevant experience required with a global mindset
  • PhD in natural sciences, medicine, pharmaceutical sciences
  • Generalist in Medical Affairs with knowledge in Hematology/Oncology
  • Experience in implementing Medical Affairs plans
  • Strong analytical and problem-solving capabilities
  • Excellent organizational and time management skills
  • Experience in working in matrix organizations
  • Ability to work independently and coordinate workload in a team environment, in order to meet established deadlines, under pressure
  • Team player with well-developed interpersonal abilities
  • Excellent written and oral communication skills in English, including grammatical/technical writing and presentation skills

Ihr Ansprechpartner

Tilman Grumbd
Geschäftsführer

Anschrift

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