Associate Vice President, Clinical R&D

Allozymes; Region Hovedstaden; Sur place; DKK 2 000 000 - 3 000 000; Plein temps

Résumé du poste

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

You will drive execution of the clinical development roadmap across assays, instruments, software, and integrated workflows. The role demands strategic leadership, deep experience in regulated medical devices, and a track record of delivering complex products from concept through commercialization while aligning diverse

Qualifications

• Bachelor’s or master’s degree in a relevant scientific/engineering field; advanced degree preferred.
• 10+ years of product development in medical devices/diagnostics or regulated industries.
• 7+ years of progressively responsible leadership experience.
• Experience leading global, multidisciplinary teams and launching complex products.
• Strong knowledge of medical-device/IVD development, quality systems, and regulations.
• Excellent executive communication and stakeholder management.
• Fluency in written and spoken English.

Responsabilités

• Execute the CDD Development with Clinical & Diagnostics leadership.
• Own product roadmap across assays, instruments, software, and solutions.
• Lead new product development from concept to commercialization.
• Ensure programs meet customer, clinical, technical, quality, regulatory, and schedule objectives.
• Align R&D with cross-functional teams across the organization.
• Ensure development activities comply with QMS and global IVD requirements.
• Lead portfolio investments, budgets, planning, and risk management.
• Build a high-performing global R&D organization and digitize processes.
• Represent Clinical R&D with customers, scientists, and partners.
• Engage with CTO to align with enterprise innovation initiatives.

Connaissances

Executive communication

Stakeholder management

Cross-functional leadership

Global team leadership

Strategic thinking

Formation

Bachelor or Master in scientific/engineering/software

Advanced degree preferred

Outils

Quality Management System

Regulatory processes

Design controls

Risk management

Description du poste

Job Description

The Associate Vice President of Clinical R&D will lead the global organization responsible for developing Agilent’s clinical diagnostic solutions. Based in Glostrup, this leader will drive execution of the clinical development solution roadmap across assays, instruments, software, and integrated workflows.

We are seeking a strategic, results-driven leader with a strong record of product development, organizational leadership, and execution in regulated environments.

Key Responsibilities

• Execute the CDD Development in partnership with the Clinical & Diagnostics Division leadership team.
• Own the execution of developing the product roadmap across solutions encompassing 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.
• Ensure development activities comply with Agilent’s Quality Management System and applicable global medical-device and IVD requirements.
• Lead portfolio investment, resource planning, budgets, organizational performance, and program risk management efforts.
• Build a high-performing global R&D organization, develop future leaders, and strengthen technical capabilities while driving process improvement and execution efficiencies through digitization, automation, and systems modernization
• Represent Clinical R&D with key customers, scientific leaders, and external partners.
• Deeply engage with the Agilent R&D community and Chief Technology Office team to ensure alignment and implementation with enterprise innovation initiatives

Qualifications

• Bachelor’s or master’s degree in a relevant scientific, engineering, software, or technical discipline; an advanced degree is preferred.
• At least 10 years of product-development experience in medical devices, diagnostics, life sciences, or another regulated industry.
• At least seven years of progressively responsible leadership experience.
• Demonstrated success leading global, multidisciplinary teams and launching complex products.
• Experience spanning several relevant areas, such as reagents, assays, instruments, software, systems engineering, or clinical workflows.
• Strong knowledge of medical-device or IVD development, design controls, risk management, quality systems, and applicable regulations.
• Proven strategic, financial, organizational-development, and cross-functional leadership capabilities.
• Excellent executive communication and stakeholder-management skills.
• Full professional fluency in written and spoken English.

Preferred Experience

• Clinical diagnostics development in pathology, immunohistochemistry, companion diagnostics, or other cancer diagnostics.
• Integrated hardware, software, consumable, and assay development.
• Support for global regulatory submissions and commercialization across multiple markets.
• Leading a substantial R&D organization through growth or transformation.

Additional Details

This job has a full time weekly schedule.

Our pay ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at: https://careers.agilent.com/locations

Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.

Travel Required

10% of the Time

Shift

Day

Duration

No End Date

Job Function

R&D