Global AVP, Clinical R&D — Strategy & Execution Leader

DAKO Denmark R&D & Manufacturing; Glostrup Kommune; On-site; DKK 1,000,000 - 1,500,000; Full time

Job summary

Agilent Technologies Inc. in Denmark seeks an Associate Vice President of Clinical R&D to lead the global organization developing clinical diagnostic solutions.

Based in Glostrup, this executive will drive the clinical development roadmap across assays, instruments, software, and integrated workflows while ensuring compliance with medical-device and IVD requirements. You will build a high-performing, global R&D function, align with Product Management, Quality, Regulatory, and Operations, manage

Qualifications

• Executive leadership with a track record in regulated medical-device or diagnostics development.
• Global, multidisciplinary product development experience spanning assays, instruments, software, and workflows.
• Strong stakeholder management and strategic communication across functions.

Responsibilities

• Execute the CDD Development in partnership with the Clinical & Diagnostics Division leadership team.
• Own the execution of developing the product roadmap across assays, instruments, software, and integrated solutions.
• Lead new product development from concept through design transfer, and commercialization.
• Ensure programs meet customer, clinical, technical, quality, regulatory, financial, and schedule objectives.
• Align R&D with Product Management, Marketing, Clinical Affairs, Quality, Regulatory, Operations, Supply Chain, Manufacturing, Service, and field organizations.

Skills

Executive leadership

Global team leadership

Regulated industry experience

Stakeholder management

Strategic thinking

English fluency

Education

Bachelor’s or Master’s degree in a scientific/engineering/technical discipline

Job description

Agilent Technologies Inc. in Denmark seeks an Associate Vice President of Clinical R&D to lead the global organization developing clinical diagnostic solutions.

Based in Glostrup, this executive will drive the clinical development roadmap across assays, instruments, software, and integrated workflows while ensuring compliance with medical-device and IVD requirements. You will build a high-performing, global R&D function, align with Product Management, Quality, Regulatory, and Operations, manage