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ABAbbott

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

Eschborn
VollzeitVor OrtSenior

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.

Anforderungen

  • 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)

Aufgaben

  • 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.

Berufserfahrung

  • 8 Jahre

Ausbildung

  • Master-Abschluss

Sprachen

  • Englischverhandlungssicher
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