Clinical Development Lead, CVMD — Global Diagnostics Strategy

Roche Holding AG

Wien

Vor Ort

EUR 180.000 - 240.000

Vollzeit

Vor 3 Tagen
Sei unter den ersten Bewerbenden
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Zusammenfassung

Roche Holding AG in Vienna seeks a Clinical Development Lead for Cardiovascular and Metabolic Diseases (CVMD) within Diagnostics CDMA to shape clinical strategy and global program execution. You will drive end-to-end development, define clinical utility and engage with stakeholders across functions to deliver differentiated solutions.

In this role you will lead large studies, collaborate with regulatory bodies, build partnerships with international experts, mentor the team, and set standards for

Qualifikationen

  • MD or PhD in cardiology, metabolic diseases or related field.
  • Experience in CVMD area within academia, diagnostics, or pharma.
  • Clinical trial management across global studies (IVD/Medical Device).
  • Proven leadership of large, complex development programs.
  • Deep knowledge of global standards and regulations (ICH-GCP, MDR/FDA).

Aufgaben

  • Lead clinical development strategy for large-scale CVMD studies and programs.
  • Work with Health Authorities on filings and regulatory submissions.
  • Build strategic partnerships with international KOLs and institutions.
  • Oversee communication strategies for clinical studies and publications.
  • Drive innovation, IP strategies, and optimize clinical processes.
  • Coach and mentor team members to grow expertise.

Kenntnisse

Clinical strategy
Leadership
Regulatory knowledge
Stakeholder management
Cross-functional collaboration

Ausbildung

MD or PhD in cardiology/metabolic diseases

Jobbeschreibung

Roche Holding AG in Vienna seeks a Clinical Development Lead for Cardiovascular and Metabolic Diseases (CVMD) within Diagnostics CDMA to shape clinical strategy and global program execution. You will drive end-to-end development, define clinical utility and engage with stakeholders across functions to deliver differentiated solutions.

In this role you will lead large studies, collaborate with regulatory bodies, build partnerships with international experts, mentor the team, and set standards for

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