Medical Affairs Specialist EMEA DBS

il y a 1 mois


Paris, Île-de-France Boston Scientific Temps plein
Job Title: Medical Affairs Specialist EMEA DBS

At Boston Scientific, we're committed to advancing science for life. As a Medical Affairs Specialist EMEA DBS, you'll play a critical role in building and maintaining relationships with Key Opinion Leaders, engaging them on their fields of interest and areas of strategic importance to our company.

Key Responsibilities:
  • Evaluate external clinical research proposals and collaborate with cross-functional teams to advise on how research proposals fit our overall clinical strategy.
  • Participate in the development of the EMEA clinical evidence plan, assessing gaps and needs that align with our strategic focus and drive research topics of interest.
  • Provide support for scientific rigor of all regional Boston Scientific funded research.
  • Communicate with investigators on all scientific questions prior, during, and after the review process for investigator-sponsored research, research collaborations, and ancillary research grants.
  • Stay in close contact with investigators, arranging scientific support and monitoring project progress to provide clear project status during reviews with cross-functional teams.
  • Inform relevant departments who may benefit from results or publications from supported projects, ensuring timely tracking of milestones for quarterly and annual reports.
  • Ensure clinical evidence generation supports our strategic needs regionally, with equitable participation in research from the EMEA region.
  • Develop relationships with EMEA KOLs and field personnel through scheduled meetings and other interactions.
  • Act as a scientific liaison between commercial and global scientific teams.
Requirements:
  • PhD in Neurosciences or equivalent relevant qualification.
  • Specialized knowledge of clinical issues associated with Deep Brain Stimulation.
  • Thorough knowledge of clinical research, device development process, regulatory requirements, laws, and good clinical practices.
  • Experience in running clinical trials advantageous.
  • Demonstrated ability to develop and maintain relationships with Key Opinion Leaders.
  • Demonstrated strength in developing and delivering strong, storytelling presentations.
  • Proven ability to communicate complex data to diverse audiences.
  • Demonstrated success in managing projects, particularly clinical research programs.
  • Fluent in English.
  • Willing and able to travel as required by workload (30-50%).


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