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ABAbbott

Director, Global Medical Affairs - Heart Failure(m/w/x)

Eschborn
Full-timeOn-siteSenior

Managing clinical research professionals, providing medical guidance for advanced cardiovascular product development. MD degree, 8 years clinical experience in cardiovascular disease, and 60% global travel required. Work within a dedicated cardiovascular business unit.

Requirements

  • Significant global presence (approx. 60% travel)
  • Engagement with investigators, clinical sites, and internal stakeholders
  • MD degree
  • 8 years clinical experience in cardiovascular disease area
  • Preferred: Documented medical or surgical experience treating advanced heart failure patients
  • Medical research and scientific publishing experience
  • Preferred: Industry experience
  • Fluent English
  • Additional language skills (a plus)

Tasks

  • Manage Clinical Research professionals.
  • Provide medical guidance for the business group.
  • Ensure focus on product performance and safety.
  • Support ISS, grants, and scientific activities.
  • Collaborate on clinical trial results review, implementation, and publication.
  • Contribute to establishing clinical science plans and goals.
  • Implement and maintain clinical research policies and procedures.
  • Lead product performance testing and evaluation.
  • Direct risk management activities.
  • Advise Clinical Affairs on clinical research publications, abstracts, and presentations.
  • Provide critical input for new product safety processes and procedures.
  • Manage regional ISS and Research Grant programs.
  • Develop priorities for the Global Abbott HF ISS strategy.
  • Contribute to physician education on advanced HF, MCS, and hemodynamic management.
  • Collaborate with professional societies to increase awareness and knowledge of advanced HF and hemodynamic management.
  • Assist commercial and marketing teams with strategic customer and KOL interactions.
  • Lead and deliver internal educational activities on heart failure.
  • Provide input to R&D across all product portfolio stages.
  • Support Clinical Affairs.
  • Drive Abbott-led trials.
  • Ensure regional representation in critical heart failure evidence generation.
  • Conduct off-label discussions with OUS clinicians.
  • Assist Market Access with clinical input for OUS reimbursement processes.
  • Represent Abbott HF Medical Affairs in regulatory body interactions.
  • Provide medical input to investigation teams.
  • Provide medical support for reporting to regulatory authorities.
  • Update medical affairs procedural documents and submit change requests.

Work Experience

  • 8 years

Education

  • Master's degree

Languages

  • EnglishBusiness Fluent
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Abbott and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.

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