Director, Clinical Affairs & European Evidence Strategy

Intuitive; Aubonne; On-site; CHF 180,000 - 260,000; Full time

Job summary

Intuitive is seeking a senior leader to drive European clinical evidence strategies across premarket and postmarket programs. You will collaborate with Marketing, Medical Affairs, Regulatory, and regional teams to align evidence plans with business objectives and ensure high-quality study execution.

You will build and lead a team, manage external partners, and drive PMCF, registries, and investigator-initiated studies while ensuring compliance with GCP, EU MDR, and data privacy requirements

Qualifications

• Strong knowledge of Good Clinical Practice (GCP) and EU MDR requirements.
• Experience with premarket and post-market evidence generation is preferred.
• Ability to interact effectively with physicians and regulators across Europe.
• Proven leadership of clinical affairs teams and external partners.
• Excellent project management and strategic prioritization skills.

Responsibilities

• Develop and implement European clinical evidence strategies to meet business goals.
• Collaborate with EU commercial leaders, Marketing, Medical Affairs, and Regulatory to align programs.
• Translate strategic content into clear evidence roadmaps for cross-functional teams.
• Lead and mentor Clinical Affairs staff and guide internal/external communication.
• Oversee European clinical research activities including PMCF, registries, and investigator-initiated studies.
• Engage with KOLs, hospitals, and societies to support evidence planning and dissemination.
• Ensure compliance with SOPs, GCP, EU MDR, and data protection requirements.

Skills

Clinical research

Team leadership

Regulatory knowledge

GCP

EU MDR

English fluency

Strategic thinking

Education

Advanced degree (MD/MS/PhD) in scientific/bioengineering

Job description

Intuitive is seeking a senior leader to drive European clinical evidence strategies across premarket and postmarket programs. You will collaborate with Marketing, Medical Affairs, Regulatory, and regional teams to align evidence plans with business objectives and ensure high-quality study execution.

You will build and lead a team, manage external partners, and drive PMCF, registries, and investigator-initiated studies while ensuring compliance with GCP, EU MDR, and data privacy requirements