Global Medical Affairs PDT Specialty Therapies 100% (m/f/d)

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Switzerland | 
Freelance
Job title: Global Medical Affairs PDT Specialty Therapies 100% (m/f/d)
Industry: Pharma
Skills: Medical Director, Global Medical Affairs
Start of project: 01.04.2022
Duration of the project : 6 Months
Location: Switzerland

Objectives
  • GlobalDevelop the overall medical strategy for the assigned therapeutic area in alignment with regional- and local medical functions and Medical centers of excellence.
  • Lead the execution of the PDT global medical affairs activities and help develop an integrated medical strategy in collaboration with the Medical Unit Head and Global Medical Leads for assigned therapeutic area including scientific training, field medical resource development, medical conferences, and publications.
  • Scientific lead for assimilation, dissemination and archival of all content developed for the assigned therapeutic area
  • Provide accountability for medical aspects of the Commercial – Medical – Legal – Regulatory (CMLR) promotional review process
  • Contribute to creation and management of budget for assigned area


Acountabilities
  • Lead activities within PDT Medical Affairs for one or more disease areas / assets to ensure quality and timely delivery of medical affairs activities according to the respective medical strategic plans in coordination with the Head of Medical Functions, the Medical Unit Head and Global Medical Leads.
  • Provide scientific leadership contributing to launch and life-cycle management by collaborating within the PDT Medical Affairs team for one or more disease areas / assets to translate medical strategy into medical communication plans and activities.
  • Accountable for the execution of assigned medical tactics derived from the medical plan(s).
  • As part of a matrixed team, lead and be accountable with the Medical Unit Head and Medical Leads to identify, coordinate and execute assigned activities for medical conferences including medical information booth presence, development of medical booth content, symposia, alignment of competitive intelligence, pre and post-meeting conference reporting.
  • As part of a matrixed team, lead and be accountable with the Medical Unit Head and Medical Leads to execute the publication strategy based on medical strategies, publication obligations, and data availability; collaborate with medical affairs unit, medical publications agencies and external authors to ensure execution the publication plan.
  • Ensure company-sponsored publication activities are conducted according to good publication practices (including, but not limited to ICMJE, GPP3, CONSORT, etc) and  Global Publication Standard, SOP, and applicable practice guidelines. Track, and report publications metrics as required.
  • Provide oversight of agency partners to ensure appropriate execution of publication plans; ensure vendor partners are properly trained on company standards, SOPs, systems, and tools for appropriate and effective execution of responsibilities, including interactions with alliance partners, authors (internal and external), as well as company data-generators, and reviewers.
  • Closely coordinate budget reporting; responsible for appropriate tracking and reporting of transfer of value according to applicable transparency rules and regulations.
  • As part of a matrixed team, lead and be accountable with the Medical Unit Head and Global Medical Leads, to develop internal and external materials for use by medical teams and ensure assimilation, dissemination and archival of content created for the assigned therapeutic area.
  • In collaboration with the PDT Medical Affairs team, provide input for the planning and monitoring of medical activities according to the integrated medical strategy for assigned area and provide operational budget oversight for disease areas/assets in alignment with other relevant internal stakeholders (e.g. Finance).
  • Lead and be accountable for resolving CMLR questions and provide leadership in concept design and approval of promotional and non-promotional materials.


Qualifications

  • A relevant degree is required. A medical or scientific degree (MD, PharmD,  PhD, MS or RN) is preferred.
  • Experience with plasma derived pharmaceuticals, pulmonology or rare disease is preferred.
  • >12 years of experience in the biopharmaceutical industry, preferably within a matrix structure.
  • >5 years of experience within medical affairs roles (e.g. Medical Science Liaison, Medical Information, Medical Communications, Medical Education, Publications).
  • Experience leading teams is desirable.
  • Experience managing vendors and complex projects is required.
  • Strong knowledge of international regulatory and legal guidelines regarding medical communication/publication approaches as well as best practices is required.


Referenznummer:
Branche:
Beginn des Projekts:
Dauer:
Anstellungsart:
Kontakt
Moritz Janssen
m.janssen@aristo-group.ch
+41 44 274 39 00
11135
Pharma
01.04.2022
6 Months
Freelance
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