14 дней назад
Associate Vice President, Clinical R&D (Clinical Diagnostics)
Вакансия из Hirify Global, списка международных tech-компанийДля мэтча и отклика нужен Plus
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Associate Vice President, Clinical R&D (Clinical Diagnostics): Leading global development of clinical diagnostic solutions spanning assays, instruments, software, and integrated workflows with an accent on regulated product development, quality, regulatory, and cross-functional execution. Focus on launching complex products, building a high-performing global R&D organization, managing portfolio investment and risk, and driving digitization and systems modernization.
Location: Glostrup, Denmark
Company
develops clinical diagnostic solutions across assays, instruments, software, and integrated workflows.
What you will do
- Lead execution of the clinical development roadmap across assays, instruments, software, and integrated solutions.
- Direct 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, manufacturing, supply chain, service, and field organizations.
- Manage portfolio investment, resources, budgets, organizational performance, and program risks.
- Build a high-performing global R&D organization while advancing technical capabilities, digitization, automation, and systems modernization.
Requirements
- 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.
- Experience leading global, multidisciplinary teams and launching complex products across 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.
- Full professional fluency in written and spoken English is required.
Nice to have
- Clinical diagnostics experience in pathology, immunohistochemistry, companion diagnostics, or cancer diagnostics.
- Experience with integrated hardware, software, consumable, and assay development.
- Experience supporting global regulatory submissions and commercialization across multiple markets.
- Experience leading a substantial R&D organization through growth or transformation.
Culture & Benefits
- Full-time schedule with daytime working hours.
- Global collaboration with customers, scientific leaders, external partners, the R&D community, and the Chief Technology Office.
- Approximately 10% travel required.
- Compensation and benefits vary by work location, role level, skills, experience, and education.
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