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12 дней назад

Clinical Development Lead (Cardiovascular and Metabolic Diseases)

Формат работы
onsite
Тип работы
fulltime
Грейд
lead
Английский
b2
Страна
Austria
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Clinical Development Lead (Cardiovascular and Metabolic Diseases) (Diagnostics/Clinical Development): Leading clinical development strategies for large-scale cardiovascular and metabolic disease studies and diagnostic solutions with an accent on clinical utility, global regulatory submissions, and evidence generation. Focus on designing and managing complex IVD and medical device trials, guiding cross-functional programs, engaging health authorities and key opinion leaders, and developing clinical communication strategies.

Location: Vienna, Austria; the role is based at the Vienna office

Company

hirify.global GmbH, acquired by Roche, develops digital health, diagnostic, and healthcare solutions through Roche Diagnostics Solutions.

What you will do

  • Lead clinical development strategies for large-scale studies and complex cardiovascular and metabolic disease programs.
  • Define clinical utility, intended use, and claim extensions across the product portfolio.
  • Partner with Global Regulatory Affairs on global regulatory filings, meeting packages, and clinical documentation.
  • Represent the medical function with health authorities, key opinion leaders, industry partners, and academic institutions.
  • Oversee clinical study communications, congress participation, advisory boards, and scientific publications.
  • Coach team members while driving innovation, intellectual property strategies, and clinical process improvements.

Requirements

  • Medical degree or PhD in cardiology, metabolic diseases, obesity, or a related field.
  • Established experience in academia, diagnostics, or the pharmaceutical industry within the cardiovascular and metabolic disease area.
  • Proven experience managing global in vitro diagnostics or medical device studies, including protocol design and clinical report writing.
  • Experience leading large, complex development programs and cross-functional matrix teams.
  • Strong knowledge of ICH-GCP, IVDD/IVDR, MDR, FDA, and NMPA standards and regulations.
  • Ability to collaborate across diverse regions, cultures, and time zones.

Culture & Benefits

  • Inclusive, collaborative, and patient-centered working environment.
  • Family-friendly career paths and a focus on sustainability and healthy lifestyles.
  • Modern workplace flexibility, learning, knowledge sharing, and open feedback.
  • Opportunities for professional and personal development.
  • Work focused on improving diagnosis, patient care, and healthcare sustainability.

Hiring process

  • Submit a CV in English through the application process.

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