Clinical Development Lead

ITech Consult AG; Madrid; Presencial; EUR 120.000 - 180.000; Jornada completa

Descripción de la vacante

ITech Consult AG is seeking a Clinical Development Lead - Cardiovascular to shape the clinical strategy for global CVMD trials in diagnostics. You will partner with Regulatory Affairs for filings, engage with health authorities and KOLs, and lead cross-functional teams across clinical operations.

The role requires extensive experience in IVD/medical device trials, strong leadership, and a track record of delivering complex development programs across regions. Travel up to 25% is expected.

Formación

• MD or PhD in cardiology, metabolic diseases, obesity or related field.
• Proven experience in CVMD areas within academia, diagnostics, or pharma.

Responsabilidades

• Define clinical development strategy for large-scale CVMD studies and programs.
• Collaborate with regulatory affairs for global filings and submissions.
• Lead external interactions with health authorities and KOLs.
• Oversee communications for clinical studies, congresses, and publications.
• Drive innovation, IP strategies, and optimization of clinical processes.
• Mentor and coach team members to develop expertise.

Conocimientos

Clinical strategy

Regulatory knowledge

Program leadership

Cross-functional collaboration

IVD trials

KOL engagement

Educación

MD or PhD in cardiology/related field

Descripción del empleo

Clinical Development Lead- Cardiovascular: Clinical Strategy /Global Clinical Trials / Medical Device study management / ICH-GCP / IVDD/IVDR / MDR / FDA / NMPA /English

¿Tiene las siguientes habilidades, experiencia e impulso para tener éxito en este puesto? Descúbralo a continuación.

Background:

Are you ready to shape the future of healthcare by leading the clinical development strategy for next generation diagnostic solutions? As a Clinical Development Lead, Cardiovascular and metabolic diseases (CVMD) within our Clinical and Medical Affairs organization in Diagnostics, you will play a pivotal role in planning and implementing clinical development activities that bring medically-differentiated solutions to patients globally. In this role, you will act as a senior strategic voice and trusted advisor, fostering an environment where science and collaboration thrive.

Key Responsibilities:

• Drive Clinical Strategy: Lead the clinical development strategy for large-scale studies and complex programs, in the CVMD area, defining clinical utility, intended use, and claim extensions across our portfolio.
• Lead Health Authority Interactions: Work closely with Global Regulatory Affairs in the completion and submission of global regulatory filings, authoring critical sections of meeting packages and reviewing clinical documents for international regulatory submissions.
• Forge Stakeholder Partnerships: Act as the medical lead in external interactions with health authorities, build strategic relationships with international Key Opinion Leaders (KOLs), and drive development partnerships across industry and academia.
• Foster Communication Excellence: Oversee the implementation of communication strategies for clinical studies, representing the organization at major medical congresses, advisory boards, and in key publications.
• Champion Innovation & Excellence: Act as a key driver for competitive differentiation, innovation, and early pipeline activities while developing intellectual property strategies and optimizing clinical processes.
• Coach and Mentor: Act as a dedicated coach for team members, nurturing confidence and helping colleagues develop their skills and expertise.

Must Haves:

• Medical degree (MD) or an advanced degree (PhD) in cardiology, metabolic diseases, obesity or related fields.
• Established experience within academia, diagnostics, or the pharmaceutical industry, in the CVMD area.
• Clinical Expertise: Proven track record in In Vitro Diagnostics (IVD) or Medical Device study management across all stages of global clinical trials, including protocol design and report writing.
• Program Leadership: Demonstrated experience leading large, complex development programs and guiding cross-functional, matrixed teams.
• Regulatory Knowledge: Deep understanding of applicable global standards and regulations, such as ICH-GCP, IVDD/IVDR, MDR, FDA, and NMPA.
• Inclusion & Collaboration: Ability to partner effectively across diverse regions, cultures, and time zones to foster an environment of belonging and collaboration. xqysrnh
• Travel: Willingness to travel up to 25% depending on project phases.

Referenz Nr.: 925235

Rolle: Clinical Development Lead- Cardiovascular

Industrie: Pharma

Work Location: Spain/Austria

Workload: 100%

Start Datum: ASAP

Duration: 12++ Months with a possibility of extension

Deadline : 22/09/2026