Your role:
- Support the evaluation of innovative (AI) solutions and technologies, contributing to the assessment of their potential to address identified needs and challenges.
- Develop clinical evaluation documentation supporting regulatory submissions and post-market clinical surveillance strategy.
- Define and execute (internal and external) clinical and performance studies, leading in protocol development, data collection, and analysis, ensuring robust scientific methodologies.
- Perform quality reviews, tracking, document control, and management of essential study, clinical evaluation and clinical post market documents.
- Assist in the preparation of strategic thought leadership materials, including reports, presentations, and publications, to support marketing strategies and organizational objectives.
- Act as author for documentation and publications resulting from clinical studies, literature reviews, and other research related activities, sharing insights and findings with relevant stakeholders to advance knowledge and drive impact.
- Conduct research to identify emerging customer needs and trends within the specified domain of diagnosis, treatment, and patient care, informing strategic decision-making and product development initiatives.
- Implement research initiatives, including intellectual property (IP) assessment, contributing to the development and execution of research protocols.
You're the right fit if:
- PhD Degree in Biotechnology, Pharmacology, Biomedical Sciences, Artificial Intelligence, or an equivalent field (preferred).
- Master's Degree in Biotechnology, Pharmacology, Biomedical Sciences, Artificial Intelligence, or an equivalent field, with a strong understanding of research methodologies, clinical study design according to Good Clinical Practices (GCP), and Statistics.
- Additionally, demonstrated relevant experience in technical domains such as advanced image processing, Artificial Intelligence, or nuclear medicine is preferred
- At least 3 years of experience in areas such as Clinical Research or Clinical Trials, preferably within the Medical Devices or Pharmaceutical Industry, or an equivalent field. With a PhD, No prior experience required.
- Strong knowledge of Biostatistics.
- Basic understanding of medical imaging or imaging pros-process (is a plus).
- Experience as a medical/scientific writer or in an equivalent role.
- Knowledge of regulatory processes (preferred).
We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help the lives of others.
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If you’re interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our culture of impact with care .